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dbVar

Database of genomic structural variation

nsv5625594

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: 89 SVs from 24 studies. See in: genome view

Submitted genomic14,913,058-14,913,058

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5625594	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	14,913,058	14,913,058
nsv5625594	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	14,955,057	14,955,057

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17069213	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
nssv17069213	Submitted genomic		NC_000010.11:g.149 13058_14913059ins1 75	GRCh38 (hg38)		NC_000010.11	Chr10	14,913,058	14,913,058
nssv17069213	Remapped	Perfect	NC_000010.10:g.149 55057_14955058ins1 75	GRCh37.p13	First Pass	NC_000010.10	Chr10	14,955,057	14,955,057

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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