A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3565453



Internal ID18863734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:53816432..53896009hg38UCSC Ensembl
Innerchr18:51342802..51422379hg19UCSC Ensembl
Innerchr18:49596800..49676377hg18UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3879578
hg1979578
hg1879578
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058867
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)nssv3565453
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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