A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3565631



Internal ID18863912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:64450019..64590176hg38UCSC Ensembl
Innerchr18:62117254..62257411hg19UCSC Ensembl
Innerchr18:60268234..60408391hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38140158
hg19140158
hg18140158
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057778
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)nssv3565631
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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