A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564118



Internal ID18862399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14071214..14304890hg38UCSC Ensembl
Innerchr18:14071213..14304889hg19UCSC Ensembl
Innerchr18:14061213..14294889hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38233677
hg19233677
hg18233677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066363
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)nssv3564118
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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