A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17044039



Internal ID97092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32998272..33025635hg38UCSC Ensembl
chr11:33019818..33047181hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3827364
hg1927364
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5496693
Supporting Variants
Samples
Known GenesDEPDC7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17044039
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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