A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060311



Internal ID18802842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54756764..54867988hg38UCSC Ensembl
Innerchr19:55268216..55379443hg19UCSC Ensembl
Innerchr19:59960028..60071255hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38111225
hg19111228
hg18111228
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3668n100
Supporting Variantsnssv3570220
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)nsv1060311
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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