A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149825



Internal ID15528542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1525308..1550651hg38UCSC Ensembl
Innerchr19:1525307..1550650hg19UCSC Ensembl
Innerchr19:1476307..1501650hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3825344
hg1925344
hg1825344
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578297
Supporting Variants
SamplesHGDP00654
Known GenesPLK5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149825
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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