A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv887395



Internal ID16181351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:76390991..76394780hg38UCSC Ensembl
Innerchr18:74102947..74106736hg19UCSC Ensembl
Innerchr18:72231935..72235724hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg383790
hg193790
hg183790
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577667
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)nssv887395
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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