A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17052139



Internal ID102608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96370217..96370336hg38UCSC Ensembl
chr11:96103381..96103500hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5498179
Supporting Variants
Samples
Known GenesCCDC82
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17052139
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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