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dbVar

Database of genomic structural variation

nsv6006110

Organism: Homo sapiens

Study:nstd212 (Wu et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:2,731

Publication(s):Wu et al. 2021

Links to Other Resources

Overlapping Genes

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: 88 SVs from 19 studies. See in: genome view

Submitted genomic47,262,750-47,265,480

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6006110	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	47,262,750	47,265,480
nsv6006110	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	47,230,486	47,233,216

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17558205	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17558205	Submitted genomic		NC_000006.12:g.472 62750_47265480dup	GRCh38 (hg38)		NC_000006.12	Chr6	47,262,750	47,265,480
nssv17558205	Remapped	Perfect	NC_000006.11:g.472 30486_47233216dup	GRCh37.p13	First Pass	NC_000006.11	Chr6	47,230,486	47,233,216

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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