A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046475



Internal ID98787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71886022..71909696hg38UCSC Ensembl
chr11:71597068..71620742hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3823675
hg1923675
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5503431
Supporting Variants
Samples
Known GenesLOC100133315
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046475
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000938


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