A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899604



Internal ID15846874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42400501..42408251hg38UCSC Ensembl
Innerchr19:42904653..42912403hg19UCSC Ensembl
Innerchr19:47596493..47604243hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg387751
hg197751
hg187751
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579632
Supporting Variants
Samples
Known GenesLIPE, LIPE-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899604
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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