A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580339



Internal ID16021062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54930401..54940537hg38UCSC Ensembl
Innerchr19:55441769..55451905hg19UCSC Ensembl
Innerchr19:60133581..60143717hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3810137
hg1910137
hg1810137
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv901805
Samples
Known GenesNLRP7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580339
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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