A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563012



Internal ID16350421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:107551231..107594972hg38UCSC Ensembl
Innerchr13:108203579..108247320hg19UCSC Ensembl
Innerchr13:107001580..107045321hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3843742
hg1943742
hg1843742
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv819124
Samples
Known GenesFAM155A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563012
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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