A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517758



Internal ID15098365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1550651..1572370hg38UCSC Ensembl
Innerchr19:1550650..1572369hg19UCSC Ensembl
Innerchr19:1501650..1523369hg18UCSC Ensembl
Innerchr19:1501650..1523369hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3821720
hg1921720
hg1821720
hg1721720
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv653140, nssv683128, nssv673051
Samples
Known GenesMEX3D
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517758
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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