A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv901751



Internal ID15849021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54771566..54775343hg38UCSC Ensembl
Innerchr19:55283018..55286795hg19UCSC Ensembl
Innerchr19:59974830..59978607hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg383778
hg193778
hg183778
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580305
Supporting Variants
Samples
Known GenesKIR2DL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv901751
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