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dbVar

Database of genomic structural variation

nsv5537278

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:1

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: 104 SVs from 20 studies. See in: genome view

Submitted genomic209,915,111-209,915,111

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5537278	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	209,915,111	209,915,111
nsv5537278	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	210,779,835	210,779,835

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16924813	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16924813	Submitted genomic		NC_000002.12:g.209 915111_209915112in s327	GRCh38 (hg38)		NC_000002.12	Chr2	209,915,111	209,915,111
nssv16924813	Remapped	Perfect	NC_000002.11:g.210 779835_210779836in s327	GRCh37.p13	First Pass	NC_000002.11	Chr2	210,779,835	210,779,835

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)
nssv16924813	0.004	25	6396

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