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

dbVar

Database of genomic structural variation

nsv5605675

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Ebert 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: 111 SVs from 24 studies. See in: genome view

Submitted genomic94,043,553-94,043,553

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5605675	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	94,043,553	94,043,553
nsv5605675	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	93,762,397	93,762,397

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17134664	insertion	SAMN00016965	Sequencing	Sequence alignment	1,475

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17134664	Submitted genomic		NC_000003.12:g.940 43553_94043554ins2 04	GRCh38 (hg38)		NC_000003.12	Chr3	94,043,553	94,043,553
nssv17134664	Remapped	Perfect	NC_000003.11:g.937 62397_93762398ins2 04	GRCh37.p13	First Pass	NC_000003.11	Chr3	93,762,397	93,762,397

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