A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525735



Internal ID15453028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:102792869..102794686hg38UCSC Ensembl
Innerchr8:103805097..103806914hg19UCSC Ensembl
Innerchr8:103874273..103876090hg18UCSC Ensembl
Innerchr8:103874273..103876090hg17UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg381818
hg191818
hg181818
hg171818
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701900
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525735
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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