A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032327



Internal ID89253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8482888..8483322hg38UCSC Ensembl
chr10:8524851..8525285hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38435
hg19435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483709
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032327
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.007025


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