A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562644



Internal ID16350053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:89776939..90233824hg38UCSC Ensembl
Innerchr13:90429193..90886078hg19UCSC Ensembl
Innerchr13:89227194..89684079hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38456886
hg19456886
hg18456886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148671
SamplesNINDS_165
Known GenesLINC00559, MIR622
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562644
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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