A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv900659



Internal ID15847929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51006470..51012759hg38UCSC Ensembl
Innerchr19:51509726..51516015hg19UCSC Ensembl
Innerchr19:56201538..56207827hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg386290
hg196290
hg186290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579961
Supporting Variants
Samples
Known GenesKLK10, KLK9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv900659
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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