A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524104



Internal ID15104711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:43889273..43897141hg38UCSC Ensembl
Innerchr13:44463409..44471277hg19UCSC Ensembl
Innerchr13:43361409..43369277hg18UCSC Ensembl
Innerchr13:43361409..43369277hg17UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg387869
hg197869
hg187869
hg177869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699979
Samples
Known GenesLACC1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524104
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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