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dbVar

Database of genomic structural variation

nsv4436473

Organism: Homo sapiens

Study:nstd102 (Clinical Structural Variants)
Variant Type:complex substitution
Method Type:Multiple
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: Yes
Region Size:239,448

Description:Single allele AND Ductal breast carcinoma

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: 3559 SVs from 106 studies. See in: genome view

Remapped(Score: Perfect):31,117,423-31,356,870

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4436473	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	31,117,423	31,356,870
nsv4436473	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000006.11	Chr6	31,085,200	31,324,647

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv15754755	complex substitution	Multiple	Multiple	Ductal breast carcinoma	Uncertain significance	ClinVar	RCV000207259.1, VCV000221339.1

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv15754755	Remapped	Perfect	GRCh38.p12	First Pass	NC_000006.12	Chr6	31,117,423	31,356,870
nssv15754755	Submitted genomic		GRCh37 (hg19)		NC_000006.11	Chr6	31,085,200	31,324,647

No validation data were submitted for this variant

Clinical Assertions

Variant Call ID	Type	Allele Origin	Subject Phenotype	Clinical Interpretation	Source of Interpretation	ClinVar ID
nssv15754755	complex substitution	somatic	Ductal breast carcinoma	Uncertain significance	ClinVar	RCV000207259.1, VCV000221339.1

No genotype data were submitted for this variant

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