A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564112



Internal ID18862393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14071214..14227776hg38UCSC Ensembl
Innerchr18:14071213..14227775hg19UCSC Ensembl
Innerchr18:14061213..14217775hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38156563
hg19156563
hg18156563
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063794
Supporting Variants
Samples
Known GenesANKRD20A5P, ZNF519
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564112
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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