A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv884929



Internal ID16178885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:60600610..60649112hg38UCSC Ensembl
Innerchr18:58267843..58316345hg19UCSC Ensembl
Innerchr18:56418823..56467325hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3848503
hg1948503
hg1848503
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577068
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv884929
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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