A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579966



Internal ID16020689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51572369..51627866hg38UCSC Ensembl
Innerchr19:52075622..52131119hg19UCSC Ensembl
Innerchr19:56767434..56822931hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3855498
hg1955498
hg1855498
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv900666
Samples
Known GenesFLJ30403, SIGLEC5, ZNF175
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579966
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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