A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563014



Internal ID16350423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:107827880..107851600hg38UCSC Ensembl
Innerchr13:108480228..108503948hg19UCSC Ensembl
Innerchr13:107278229..107301949hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3823721
hg1923721
hg1823721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv819125
Samples
Known GenesFAM155A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563014
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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