A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17029175



Internal ID87146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11711966..11713302hg38UCSC Ensembl
chr10:11753965..11755301hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381337
hg191337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483882
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17029175
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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