A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv901393



Internal ID15848663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54054505..54056824hg38UCSC Ensembl
Innerchr19:54557759..54560078hg19UCSC Ensembl
Innerchr19:59249571..59251890hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg382320
hg192320
hg182320
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580146
Supporting Variants
Samples
Known GenesVSTM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv901393
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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