A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv901405



Internal ID16195361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54219677..54242931hg38UCSC Ensembl
Innerchr19:54723546..54746780hg19UCSC Ensembl
Innerchr19:59415358..59438592hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3823255
hg1923235
hg1823235
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580154
Supporting Variants
Samples
Known GenesLILRA6, LILRB3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv901405
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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