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dbVar

Database of genomic structural variation

nsv5659446

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: 163 SVs from 33 studies. See in: genome view

Submitted genomic78,132,272-78,132,272

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5659446	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	78,132,272	78,132,272
nsv5659446	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	78,424,614	78,424,614

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17088508	insertion	HG00512	Sequencing	Sequence alignment	6,637

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17088508	Submitted genomic		NC_000015.10:g.781 32272_78132273ins1 65	GRCh38 (hg38)		NC_000015.10	Chr15	78,132,272	78,132,272
nssv17088508	Remapped	Perfect	NC_000015.9:g.7842 4614_78424615ins16 5	GRCh37.p13	First Pass	NC_000015.9	Chr15	78,424,614	78,424,614

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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