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dbVar

Database of genomic structural variation

nsv5549533

Organism: Homo sapiens

Study:nstd206 (Byrska-Bishop et al. 2022)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:28

Publication(s):Byrska-Bishop et al. 2022

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: 90 SVs from 13 studies. See in: genome view

Submitted genomic111,642,868-111,642,895

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5549533	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	111,642,868	111,642,895
nsv5549533	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	111,513,592	111,513,619

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17050219	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17050219	Submitted genomic		NC_000011.10:g.111 642868_111642895in s88	GRCh38 (hg38)		NC_000011.10	Chr11	111,642,868	111,642,895
nssv17050219	Remapped	Perfect	NC_000011.9:g.1115 13592_111513619ins 88	GRCh37.p13	First Pass	NC_000011.9	Chr11	111,513,592	111,513,619

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv17050219	0.026	164	6396

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