A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3574666



Internal ID18526261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54756764..54852057hg38UCSC Ensembl
Innerchr19:55268216..55363512hg19UCSC Ensembl
Innerchr19:59960028..60055324hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3895294
hg1995297
hg1895297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060745
Supporting Variants
Samples
Known GenesKIR2DL1, KIR2DL4, KIR2DS4, KIR3DL1, KIR3DL2, LOC100287534
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3574666
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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