A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661607



Internal ID15051573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54792856..54861907hg38UCSC Ensembl
Innerchr19:55304308..55373362hg19UCSC Ensembl
Innerchr19:59996120..60065174hg18UCSC Ensembl
Innerchr19:59996120..60065174hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3869052
hg1969055
hg1869055
hg1769055
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517143
Supporting Variants
Samples
Known GenesKIR2DL4, KIR2DS4, KIR3DL1, KIR3DL2, LOC100287534
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661607
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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