A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580327



Internal ID16021050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54790175..54815284hg38UCSC Ensembl
Innerchr19:55301627..55326739hg19UCSC Ensembl
Innerchr19:59993439..60018551hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3825110
hg1925113
hg1825113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv901785, nssv901786
Samples
Known GenesKIR2DL4, LOC100287534
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580327
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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