A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3726068



Internal ID19024349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:44280005..44415658hg38UCSC Ensembl
Innerchr18:41859970..41995623hg19UCSC Ensembl
Innerchr18:40113968..40249621hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg38135654
hg19135654
hg18135654
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056290
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3726068
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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