A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv901801



Internal ID15849071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54791531..54881299hg38UCSC Ensembl
Innerchr19:55302983..55392755hg19UCSC Ensembl
Innerchr19:59994795..60084567hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3889769
hg1989773
hg1889773
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580335
Supporting Variants
Samples
Known GenesFCAR, KIR2DL4, KIR2DS4, KIR3DL1, KIR3DL2, LOC100287534
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv901801
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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