A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039870



Internal ID94302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101908109..101909077hg38UCSC Ensembl
chr10:103667866..103668834hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38969
hg19969
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485079
Supporting Variants
Samples
Known GenesC10orf76
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039870
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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