A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150583



Internal ID15506627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:3748286..3801031hg38UCSC Ensembl
Innerchr18:3748286..3801031hg19UCSC Ensembl
Innerchr18:3738286..3791031hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3852746
hg1952746
hg1852746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576317
Supporting Variants
Samples1780854081_A
Known GenesDLGAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150583
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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