A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571638



Internal ID16012361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21609226..21728953hg38UCSC Ensembl
Innerchr16:21620547..21740274hg19UCSC Ensembl
Innerchr16:21528048..21647775hg18UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38119728
hg19119728
hg18119728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4947n54
Supporting Variantsnssv853113
Samples
Known GenesIGSF6, METTL9, OTOA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571638
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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