A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571633



Internal ID16012356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21593859..21728953hg38UCSC Ensembl
Innerchr16:21605180..21740274hg19UCSC Ensembl
Innerchr16:21512681..21647775hg18UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38135095
hg19135095
hg18135095
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4947n54
Supporting Variantsnssv853105, nssv1149630
SamplesHGDP00727
Known GenesIGSF6, METTL9, OTOA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571633
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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