A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524470



Internal ID15451763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54662761..54671963hg38UCSC Ensembl
Innerchr19:55174213..55183414hg19UCSC Ensembl
Innerchr19:59866025..59875226hg18UCSC Ensembl
Innerchr19:59866025..59875226hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg389203
hg199202
hg189202
hg179202
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700408
Samples
Known GenesLILRB4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524470
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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