A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv878499



Internal ID15825769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:26159061..26340350hg38UCSC Ensembl
Innerchr18:23739025..23920314hg19UCSC Ensembl
Innerchr18:21993023..22174312hg18UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38181290
hg19181290
hg18181290
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576576
Supporting Variants
Samples
Known GenesPSMA8, TAF4B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv878499
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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