A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516569



Internal ID15443862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54600262..54651887hg38UCSC Ensembl
Innerchr19:55111727..55163337hg19UCSC Ensembl
Innerchr19:59803539..59855149hg18UCSC Ensembl
Innerchr19:59803539..59855149hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3851626
hg1951611
hg1851611
hg1751611
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698613, nssv679756, nssv669245, nssv698489, nssv702424
Samples
Known GenesLILRA1, LILRB1, MIR8061
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516569
Frequency
Sample Size2026
Observed Gain2
Observed Loss3
Observed Complex0
Frequencyn/a


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