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dbVar

Database of genomic structural variation

nsv5973997

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Almarri et al. 2020

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: 111 SVs from 29 studies. See in: genome view

Submitted genomic36,055,104-36,055,104

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5973997	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	36,055,104	36,055,104
nsv5973997	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	36,076,654	36,076,654

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17365474	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17365474	Submitted genomic		NC_000011.10:g.360 55104_36055105ins4 63	GRCh38 (hg38)		NC_000011.10	Chr11	36,055,104	36,055,104
nssv17365474	Remapped	Perfect	NC_000011.9:g.3607 6654_36076655ins46 3	GRCh37.p13	First Pass	NC_000011.9	Chr11	36,076,654	36,076,654

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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