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

dbVar

Database of genomic structural variation

nsv5663644

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: 331 SVs from 41 studies. See in: genome view

Submitted genomic1,164,606-1,164,606

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5663644	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	1,164,606	1,164,606
nsv5663644	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	1,164,605	1,164,605

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17103821	insertion	SAMN00004622	Sequencing	Sequence alignment	1,208

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17103821	Submitted genomic		NC_000019.10:g.116 4606_1164607ins124	GRCh38 (hg38)		NC_000019.10	Chr19	1,164,606	1,164,606
nssv17103821	Remapped	Perfect	NC_000019.9:g.1164 605_1164606ins124	GRCh37.p13	First Pass	NC_000019.9	Chr19	1,164,605	1,164,605

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