A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527908



Internal ID15455201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54285412..54385273hg38UCSC Ensembl
Innerchr19:54789266..54896877hg19UCSC Ensembl
Innerchr19:59481078..59588689hg18UCSC Ensembl
Innerchr19:59481078..59588689hg17UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3899862
hg19107612
hg18107612
hg17107612
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704414
Samples
Known GenesLAIR1, LILRA3, LILRA4, LILRA5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527908
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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