A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17710269



Internal ID133935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85277800..85284682hg38UCSC Ensembl
chr16:85311406..85318288hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg386883
hg196883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5531873
Supporting Variants
Samples
Known GenesLINC00311
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17710269
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000158


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