A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564072



Internal ID18515667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:4356108..4505125hg38UCSC Ensembl
Innerchr18:4356108..4505125hg19UCSC Ensembl
Innerchr18:4346108..4495125hg18UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38149018
hg19149018
hg18149018
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061891
Supporting Variants
Samples
Known GenesDLGAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564072
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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