A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526003



Internal ID15453296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:92744402..92751530hg38UCSC Ensembl
Innerchr13:93396655..93403783hg19UCSC Ensembl
Innerchr13:92194656..92201784hg18UCSC Ensembl
Innerchr13:92194656..92201784hg17UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg387129
hg197129
hg187129
hg177129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702229
Samples
Known GenesGPC5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526003
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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