A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528370



Internal ID15455663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54247206..54284902hg38UCSC Ensembl
Innerchr19:54751065..54788756hg19UCSC Ensembl
Innerchr19:59442877..59480568hg18UCSC Ensembl
Innerchr19:59442877..59480568hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3837697
hg1937692
hg1837692
hg1737692
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704957
Samples
Known GenesLILRB2, LILRB5, MIR4752
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528370
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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