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dbVar

Database of genomic structural variation

nsv5553829

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:24

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: 172 SVs from 33 studies. See in: genome view

Submitted genomic17,690,298-17,690,321

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5553829	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	17,690,298	17,690,321
nsv5553829	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	17,690,529	17,690,552

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16979223	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16979223	Submitted genomic		NC_000006.12:g.176 90298_17690321ins5 4	GRCh38 (hg38)		NC_000006.12	Chr6	17,690,298	17,690,321
nssv16979223	Remapped	Perfect	NC_000006.11:g.176 90529_17690552ins5 4	GRCh37.p13	First Pass	NC_000006.11	Chr6	17,690,529	17,690,552

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)
nssv16979223	0.088	554	6330

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