A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3726567



Internal ID19024848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54645876..54664828hg38UCSC Ensembl
Innerchr19:55157325..55176279hg19UCSC Ensembl
Innerchr19:59849137..59868091hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3818953
hg1918955
hg1818955
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064009
Supporting Variants
Samples
Known GenesLILRB4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3726567
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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