A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578735



Internal ID16366144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:16033776..16061929hg38UCSC Ensembl
Innerchr19:16144586..16172739hg19UCSC Ensembl
Innerchr19:16005586..16033739hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3828154
hg1928154
hg1828154
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149847
SamplesHGDP01169
Known GenesLINC00905
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578735
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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