A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv887404



Internal ID16181360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:76392971..76394384hg38UCSC Ensembl
Innerchr18:74104927..74106340hg19UCSC Ensembl
Innerchr18:72233915..72235328hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381414
hg191414
hg181414
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577668
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)nssv887404
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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