A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3319n54



Internal ID22771214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91476440..91598200hg38UCSC Ensembl
chr13:92128694..92250454hg19UCSC Ensembl
chr13:90926695..91048455hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38121761
hg19121761
hg18121761
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv562716, nsv562717
Samples
Known GenesGPC5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3319n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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