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dbVar

Database of genomic structural variation

nsv4457709

Organism: Homo sapiens

Study:nstd102 (Clinical Structural Variants)
Variant Type:copy number variation
Method Type:Multiple
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: Yes
Region Size:954,263

Description:GRCh37/hg19 20p11.23-11.22(chr20:20817608-21771865)x3 AND not provided

Links to Other Resources

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 2161 SVs from 80 studies. See in: genome view

Remapped(Score: Good):20,836,965-21,791,227

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4457709	Remapped	Good	GRCh38.p12	Primary Assembly	First Pass	NC_000020.11	Chr20	20,836,965	21,791,227
nsv4457709	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000020.10	Chr20	20,817,608	21,771,865

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID	Copy number
nssv15775332	copy number gain	Multiple	Multiple	not provided	Uncertain significance	ClinVar	RCV000847145.2, VCV000686437.2	3

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15775332	Remapped	Good	NC_000020.11:g.(?_ 20836965)_(2179122 7_?)dup	GRCh38.p12	First Pass	NC_000020.11	Chr20	20,836,965	21,791,227
nssv15775332	Submitted genomic		NC_000020.10:g.(?_ 20817608)_(2177186 5_?)dup	GRCh37 (hg19)		NC_000020.10	Chr20	20,817,608	21,771,865

No validation data were submitted for this variant

Clinical Assertions

Variant Call ID	HGVS	Type	Allele Origin	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID	Copy number
nssv15775332	GRCh37: NC_000020.10:g.(?_20817608)_(21771865_?)dup	copy number gain	unknown	not provided	Uncertain significance	ClinVar	RCV000847145.2, VCV000686437.2	3

No genotype data were submitted for this variant

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