A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2844233



Internal ID15464139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54764800..54834857hg38UCSC Ensembl
Innerchr19:55276252..55346312hg19UCSC Ensembl
Innerchr19:59968064..60038124hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3870058
hg1970061
hg1870061
Variant TypeCNV gain
Copy Number16
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514902
Supporting Variants
SamplesNA21686
Known GenesKIR2DL1, KIR2DL4, KIR2DS4, KIR3DL1, LOC100287534
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2844233
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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