A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv887491



Internal ID16181447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:76392971..76407462hg38UCSC Ensembl
Innerchr18:74104927..74119418hg19UCSC Ensembl
Innerchr18:72233915..72248406hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3814492
hg1914492
hg1814492
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577672
Supporting Variants
Samples
Known GenesZNF516
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv887491
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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