A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563257



Internal ID16350666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113004794..113079021hg38UCSC Ensembl
Innerchr13:113659108..113733335hg19UCSC Ensembl
Innerchr13:112707109..112781336hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3874228
hg1974228
hg1874228
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3424n54
Supporting Variantsnssv820440
Samples
Known GenesMCF2L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563257
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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