A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058874



Internal ID18801405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54739639..54862351hg38UCSC Ensembl
Innerchr19:55251085..55373806hg19UCSC Ensembl
Innerchr19:59942897..60065618hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38122713
hg19122722
hg18122722
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3667n100
Supporting Variantsnssv3574619, nssv3726593
Samples
Known GenesKIR2DL1, KIR2DL3, 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)nsv1058874
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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