A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577667



Internal ID16365076
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+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv887395, nssv887400, nssv887398, nssv887403, nssv887402, nssv887394, nssv887397, nssv887393, nssv887401, nssv887396, nssv887399, nssv887392
Samples
Known GenesZNF516
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577667
Frequency
Sample Size17421
Observed Gain11
Observed Loss1
Observed Complex0
Frequencyn/a


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