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dbVar

Database of genomic structural variation

nsv5662764

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: 126 SVs from 18 studies. See in: genome view

Submitted genomic39,413,589-39,413,589

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5662764	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	39,413,589	39,413,589
nsv5662764	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	39,904,229	39,904,229

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17104712	insertion	SAMN00007703	Sequencing	Sequence alignment	1,054

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17104712	Submitted genomic		NC_000019.10:g.394 13589_39413590ins5 18	GRCh38 (hg38)		NC_000019.10	Chr19	39,413,589	39,413,589
nssv17104712	Remapped	Perfect	NC_000019.9:g.3990 4229_39904230ins51 8	GRCh37.p13	First Pass	NC_000019.9	Chr19	39,904,229	39,904,229

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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