A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563377



Internal ID16350786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113433286..113436681hg38UCSC Ensembl
Innerchr13:114087601..114090996hg19UCSC Ensembl
Innerchr13:113135602..113138997hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg383396
hg193396
hg183396
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3449n54
Supporting Variantsnssv820673
Samples
Known GenesADPRHL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563377
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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