A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573436



Internal ID16014159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84453450..84464082hg38UCSC Ensembl
Innerchr16:84487056..84497688hg19UCSC Ensembl
Innerchr16:83044557..83055189hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3810633
hg1910633
hg1810633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149337
Samples1798860279_A
Known GenesATP2C2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573436
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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