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dbVar

Database of genomic structural variation

nsv5985695

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:142,857

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: 545 SVs from 69 studies. See in: genome view

Submitted genomic115,776,069-115,918,925

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5985695	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	115,776,069	115,918,925
nsv5985695	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	116,533,645	116,676,501

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17530629	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17530629	Submitted genomic		NC_000002.12:g.115 776069_115918925du p	GRCh38 (hg38)		NC_000002.12	Chr2	115,776,069	115,918,925
nssv17530629	Remapped	Perfect	NC_000002.11:g.116 533645_116676501du p	GRCh37.p13	First Pass	NC_000002.11	Chr2	116,533,645	116,676,501

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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