A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577686



Internal ID16365095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:76476812..76521109hg38UCSC Ensembl
Innerchr18:74188768..74233066hg19UCSC Ensembl
Innerchr18:72317756..72362054hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3844298
hg1944299
hg1844299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6076n54
Supporting Variantsnssv887536
Samples
Known GenesFLJ44313, ZNF516
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577686
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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