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dbVar

Database of genomic structural variation

nsv5661505

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: 139 SVs from 13 studies. See in: genome view

Submitted genomic44,873,900-44,873,900

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5661505	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	44,873,900	44,873,900
nsv5661505	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	42,951,268	42,951,268

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17089564	insertion	HG02587	Sequencing	Sequence alignment	2,330

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17089564	Submitted genomic		NC_000017.11:g.448 73900_44873901ins1 87	GRCh38 (hg38)		NC_000017.11	Chr17	44,873,900	44,873,900
nssv17089564	Remapped	Perfect	NC_000017.10:g.429 51268_42951269ins1 87	GRCh37.p13	First Pass	NC_000017.10	Chr17	42,951,268	42,951,268

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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