A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573346



Internal ID16014069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81046761..81061486hg38UCSC Ensembl
Innerchr16:81080366..81095091hg19UCSC Ensembl
Innerchr16:79637867..79652592hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3814726
hg1914726
hg1814726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149310, nssv1149311, nssv1149312, nssv1149316, nssv1149313, nssv1149315, nssv1149314
SamplesHGDP00543, HGDP01232, HGDP00820, HGDP01008, HGDP00790, HGDP01386, HGDP01317
Known GenesATMIN, C16orf46
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573346
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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