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

dbVar

Database of genomic structural variation

nsv4764539

Organism: Homo sapiens

Study:nstd199 (Quan et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh37

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

Publication(s):Quan 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: 122 SVs from 24 studies. See in: genome view

Remapped(Score: Perfect):111,755,141-111,755,141

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4764539	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	111,755,141	111,755,141
nsv4764539	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000001.10	Chr1	112,297,763	112,297,763

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16271170	insertion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16271170	Remapped	Perfect	NC_000001.11:g.111 755141_111755142in s53	GRCh38.p12	First Pass	NC_000001.11	Chr1	111,755,141	111,755,141
nssv16271170	Submitted genomic		NC_000001.10:g.112 297763_112297764in s53	GRCh37 (hg19)		NC_000001.10	Chr1	112,297,763	112,297,763

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

You are here: NCBI