A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3565372



Internal ID18516967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:45201822..45239303hg38UCSC Ensembl
Innerchr18:42781787..42819268hg19UCSC Ensembl
Innerchr18:41035785..41073266hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3837482
hg1937482
hg1837482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061120
Supporting Variants
Samples
Known GenesSLC14A2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3565372
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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