A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065113



Internal ID18807644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:35441391..36065348hg38UCSC Ensembl
Innerchr18:33021355..33645311hg19UCSC Ensembl
Innerchr18:31275353..31899309hg18UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38623958
hg19623957
hg18623957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3564196
Samples
Known GenesC18orf21, GALNT1, INO80C, MIR187, MIR3975, RPRD1A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065113
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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