A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3574615



Internal ID18526210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54739639..54837236hg38UCSC Ensembl
Innerchr19:55251085..55348691hg19UCSC Ensembl
Innerchr19:59942897..60040503hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3897598
hg1997607
hg1897607
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059327
Supporting Variants
Samples
Known GenesKIR2DL1, KIR2DL3, KIR2DL4, KIR2DS4, KIR3DL1, LOC100287534
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3574615
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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