A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3565616



Internal ID18863897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:60597209..60650322hg38UCSC Ensembl
Innerchr18:58264442..58317555hg19UCSC Ensembl
Innerchr18:56415422..56468535hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3853114
hg1953114
hg1853114
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058389
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)nssv3565616
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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