A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899603



Internal ID15846873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42400501..42402589hg38UCSC Ensembl
Innerchr19:42904653..42906741hg19UCSC Ensembl
Innerchr19:47596493..47598581hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382089
hg192089
hg182089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579631
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)nssv899603
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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