A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065140



Internal ID18807671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:56860582..56900727hg38UCSC Ensembl
Innerchr18:54527813..54567958hg19UCSC Ensembl
Innerchr18:52678811..52718956hg18UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg3840146
hg1940146
hg1840146
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3565459
Samples
Known GenesWDR7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065140
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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