A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525714



Internal ID15106321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18697188..18703177hg38UCSC Ensembl
Innerchr8:18554698..18560687hg19UCSC Ensembl
Innerchr8:18598978..18604967hg18UCSC Ensembl
Innerchr8:18598978..18604967hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg385990
hg195990
hg185990
hg175990
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701876
Samples
Known GenesPSD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525714
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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