A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv891116



Internal ID16185072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:496724..499978hg38UCSC Ensembl
Innerchr19:496724..499978hg19UCSC Ensembl
Innerchr19:447724..450978hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg383255
hg193255
hg183255
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578114
Supporting Variants
Samples
Known GenesMADCAM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv891116
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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