A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524271



Internal ID15451564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:91767515..91849410hg38UCSC Ensembl
Innerchr13:92419769..92501664hg19UCSC Ensembl
Innerchr13:91217770..91299665hg18UCSC Ensembl
Innerchr13:91217770..91299665hg17UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3881896
hg1981896
hg1881896
hg1781896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700169
Samples
Known GenesGPC5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524271
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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