A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17030211



Internal ID87853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12909996..12914185hg38UCSC Ensembl
chr10:12951996..12956185hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg384190
hg194190
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5482583
Supporting Variants
Samples
Known GenesCCDC3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17030211
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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