Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv6010019

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:129,728

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: 380 SVs from 46 studies. See in: genome view

Submitted genomic59,390,450-59,520,177

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6010019	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	59,390,450	59,520,177
nsv6010019	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	60,303,009	60,432,736

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17593420	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17593420	Submitted genomic		NC_000008.11:g.593 90450_59520177dup	GRCh38 (hg38)		NC_000008.11	Chr8	59,390,450	59,520,177
nssv17593420	Remapped	Perfect	NC_000008.10:g.603 03009_60432736dup	GRCh37.p13	First Pass	NC_000008.10	Chr8	60,303,009	60,432,736

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.

You are here: NCBI