A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573536



Internal ID16014259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:87705252..87914409hg38UCSC Ensembl
Innerchr16:87738858..87948015hg19UCSC Ensembl
Innerchr16:86296359..86505516hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38209158
hg19209158
hg18209158
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150560
Samples1798860491_A
Known GenesCA5A, KLHDC4, MIR6775, SLC7A5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573536
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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