A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150656



Internal ID15530269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:50038886..50054619hg38UCSC Ensembl
Innerchr19:50542143..50557876hg19UCSC Ensembl
Innerchr19:55233955..55249688hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3815734
hg1915734
hg1815734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579914
Supporting Variants
SamplesHGDP00918
Known GenesFLJ26850, ZNF473
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150656
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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