A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046776



Internal ID98995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65756476..65757013hg38UCSC Ensembl
chr11:65523947..65524484hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38538
hg19538
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512295
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046776
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000625


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