A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515580



Internal ID15443191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:105913767..105944199hg38UCSC Ensembl
Innerchr8:106925995..106956427hg19UCSC Ensembl
Innerchr8:106995171..107025603hg18UCSC Ensembl
Innerchr8:106995171..107025603hg17UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3830433
hg1930433
hg1830433
hg1730433
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv667926, nssv663962
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515580
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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