A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3573313



Internal ID18524908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54212959..54293995hg38UCSC Ensembl
Innerchr19:54716828..54797848hg19UCSC Ensembl
Innerchr19:59408640..59489660hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3881037
hg1981021
hg1881021
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056967
Supporting Variants
Samples
Known GenesLILRA6, LILRB2, LILRB3, LILRB5, MIR4752
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3573313
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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