A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562725



Internal ID16350134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:92065477..92094861hg38UCSC Ensembl
Innerchr13:92717730..92747114hg19UCSC Ensembl
Innerchr13:91515731..91545115hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3829385
hg1929385
hg1829385
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv817476
Samples
Known GenesGPC5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562725
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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