A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032111



Internal ID89110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15673867..15673931hg38UCSC Ensembl
chr10:15715866..15715930hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141583
Supporting Variants
Samples
Known GenesITGA8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032111
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.014876


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