A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562958



Internal ID16350367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:100910655..100952196hg38UCSC Ensembl
Innerchr13:101562909..101604450hg19UCSC Ensembl
Innerchr13:100360910..100402451hg18UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3841542
hg1941542
hg1841542
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv818129
Samples
Known GenesNALCN-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562958
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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