A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3574596



Internal ID18526191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54736641..54837236hg38UCSC Ensembl
Innerchr19:55248107..55348691hg19UCSC Ensembl
Innerchr19:59939919..60040503hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38100596
hg19100585
hg18100585
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056571
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)nssv3574596
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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