A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv901649



Internal ID15848919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54738789..54778505hg38UCSC Ensembl
Innerchr19:55250254..55289957hg19UCSC Ensembl
Innerchr19:59942066..59981769hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3839717
hg1939704
hg1839704
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580252
Supporting Variants
Samples
Known GenesKIR2DL1, KIR2DL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv901649
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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