A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3565487



Internal ID18517082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:58351189..58451767hg38UCSC Ensembl
Innerchr18:56018421..56118999hg19UCSC Ensembl
Innerchr18:54169401..54269979hg18UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg38100579
hg19100579
hg18100579
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1067389
Supporting Variants
Samples
Known GenesMIR122, MIR3591, NEDD4L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3565487
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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