A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527803



Internal ID15108410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25380946..25382921hg38UCSC Ensembl
Innerchr8:25238462..25240437hg19UCSC Ensembl
Innerchr8:25294379..25296354hg18UCSC Ensembl
Innerchr8:25294379..25296354hg17UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg381976
hg191976
hg181976
hg171976
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704297
Samples
Known GenesDOCK5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527803
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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