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dbVar

Database of genomic structural variation

nsv5616097

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: 133 SVs from 27 studies. See in: genome view

Submitted genomic119,843,100-119,843,100

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5616097	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	119,843,100	119,843,100
nsv5616097	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	120,385,723	120,385,723

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17060173	insertion	HG03732	Sequencing	Sequence alignment	1,582

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17060173	Submitted genomic		NC_000001.11:g.119 843100_119843101in s61	GRCh38 (hg38)		NC_000001.11	Chr1	119,843,100	119,843,100
nssv17060173	Remapped	Perfect	NC_000001.10:g.120 385723_120385724in s61	GRCh37.p13	First Pass	NC_000001.10	Chr1	120,385,723	120,385,723

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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