A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv817587



Internal ID16111543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:97446728..97455949hg38UCSC Ensembl
Innerchr13:98098982..98108203hg19UCSC Ensembl
Innerchr13:96896983..96906204hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg389222
hg199222
hg189222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562804
Supporting Variants
Samples
Known GenesRAP2A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv817587
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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