A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3563005



Internal ID18861286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:74322174..74367381hg38UCSC Ensembl
Innerchr18:71989409..72034616hg19UCSC Ensembl
Innerchr18:70140389..70185596hg18UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3845208
hg1945208
hg1845208
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065204
Supporting Variants
Samples
Known GenesC18orf63
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3563005
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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