A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563259



Internal ID16350668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113007863..113074031hg38UCSC Ensembl
Innerchr13:113662177..113728345hg19UCSC Ensembl
Innerchr13:112710178..112776346hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3866169
hg1966169
hg1866169
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3424n54
Supporting Variantsnssv820442
Samples
Known GenesMCF2L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563259
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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