A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515603



Internal ID15443214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:96449987..96450830hg38UCSC Ensembl
Innerchr8:97462215..97463058hg19UCSC Ensembl
Innerchr8:97531391..97532234hg18UCSC Ensembl
Innerchr8:97531391..97532234hg17UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38844
hg19844
hg18844
hg17844
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664056, nssv668933, nssv656486
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515603
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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