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dbVar

Database of genomic structural variation

nsv5643653

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: 201 SVs from 26 studies. See in: genome view

Submitted genomic106,783,070-106,783,070

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5643653	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	106,783,070	106,783,070
nsv5643653	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	107,795,298	107,795,298

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17158348	insertion	SAMN00006466	Sequencing	Sequence alignment	4,625

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17158348	Submitted genomic		NC_000008.11:g.106 783070_106783071in s57	GRCh38 (hg38)		NC_000008.11	Chr8	106,783,070	106,783,070
nssv17158348	Remapped	Perfect	NC_000008.10:g.107 795298_107795299in s57	GRCh37.p13	First Pass	NC_000008.10	Chr8	107,795,298	107,795,298

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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