A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517607



Internal ID15444900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:104819999..104829009hg38UCSC Ensembl
Innerchr8:105832227..105841237hg19UCSC Ensembl
Innerchr8:105901403..105910413hg18UCSC Ensembl
Innerchr8:105901403..105910413hg17UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg389011
hg199011
hg189011
hg179011
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv654141, nssv691299
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517607
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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