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dbVar

Database of genomic structural variation

nsv5612102

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

Submitted genomic170,828,296-170,828,296

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5612102	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	170,828,296	170,828,296
nsv5612102	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	171,684,806	171,684,806

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17109666	insertion	HG02818	Sequencing	Sequence alignment	3,473

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17109666	Submitted genomic		NC_000002.12:g.170 828296_170828297in s67	GRCh38 (hg38)		NC_000002.12	Chr2	170,828,296	170,828,296
nssv17109666	Remapped	Perfect	NC_000002.11:g.171 684806_171684807in s67	GRCh37.p13	First Pass	NC_000002.11	Chr2	171,684,806	171,684,806

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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