A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562745



Internal ID16350154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:92627310..92725309hg38UCSC Ensembl
Innerchr13:93279563..93377562hg19UCSC Ensembl
Innerchr13:92077564..92175563hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3898000
hg1998000
hg1898000
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv817515
Samples
Known GenesGPC5, GPC5-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562745
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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