A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17029173



Internal ID87145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11692081..11702238hg38UCSC Ensembl
chr10:11734080..11744237hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3810158
hg1910158
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5489136
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17029173
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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