A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563266



Internal ID16350675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113074031..113109612hg38UCSC Ensembl
Innerchr13:113728345..113763926hg19UCSC Ensembl
Innerchr13:112776346..112811927hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3835582
hg1935582
hg1835582
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3427n54
Supporting Variantsnssv820449
Samples
Known GenesF7, MCF2L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563266
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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