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dbVar

Database of genomic structural variation

nsv5652554

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

Submitted genomic90,647,220-90,647,220

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5652554	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	90,647,220	90,647,220
nsv5652554	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	91,190,451	91,190,451

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17091850	insertion	SAMN00007824	Sequencing	Sequence alignment	1,699

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17091850	Submitted genomic		NC_000015.10:g.906 47220_90647221ins9 74	GRCh38 (hg38)		NC_000015.10	Chr15	90,647,220	90,647,220
nssv17091850	Remapped	Perfect	NC_000015.9:g.9119 0451_91190452ins97 4	GRCh37.p13	First Pass	NC_000015.9	Chr15	91,190,451	91,190,451

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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