A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573427



Internal ID16014150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84367244..84435705hg38UCSC Ensembl
Innerchr16:84400850..84469311hg19UCSC Ensembl
Innerchr16:82958351..83026812hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3868462
hg1968462
hg1868462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149334
SamplesHGDP00033
Known GenesATP2C2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573427
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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