A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578734



Internal ID16019457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:16005715..16038223hg38UCSC Ensembl
Innerchr19:16116525..16149033hg19UCSC Ensembl
Innerchr19:15977525..16010033hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3832509
hg1932509
hg1832509
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv895584
Samples
Known GenesLINC00661, LINC00905
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578734
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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