A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519645



Internal ID15100252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:109590088..109600771hg38UCSC Ensembl
Innerchr8:110602317..110613000hg19UCSC Ensembl
Innerchr8:110671493..110682176hg18UCSC Ensembl
Innerchr8:110671493..110682176hg17UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg3810684
hg1910684
hg1810684
hg1710684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv657959, nssv673425, nssv657328, nssv663200
Samples
Known GenesSYBU
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519645
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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