A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580323



Internal ID16021046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54785480..54815284hg38UCSC Ensembl
Innerchr19:55296932..55326739hg19UCSC Ensembl
Innerchr19:59988744..60018551hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3829805
hg1929808
hg1829808
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6579n54
Supporting Variantsnssv901777
Samples
Known GenesKIR2DL4, LOC100287534
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580323
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer