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dbVar

Database of genomic structural variation

nsv5966900

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: 116 SVs from 28 studies. See in: genome view

Submitted genomic103,583,767-103,583,767

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5966900	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	103,583,767	103,583,767
nsv5966900	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	105,343,524	105,343,524

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17362063	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17362063	Submitted genomic		NC_000010.11:g.103 583767_103583768in s265	GRCh38 (hg38)		NC_000010.11	Chr10	103,583,767	103,583,767
nssv17362063	Remapped	Perfect	NC_000010.10:g.105 343524_105343525in s265	GRCh37.p13	First Pass	NC_000010.10	Chr10	105,343,524	105,343,524

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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