A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525467



Internal ID15452760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82121014..82189880hg38UCSC Ensembl
Innerchr16:82154619..82223485hg19UCSC Ensembl
Innerchr16:80712120..80780986hg18UCSC Ensembl
Innerchr16:80712120..80780986hg17UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3868867
hg1968867
hg1868867
hg1768867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701595
Samples
Known GenesMPHOSPH6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525467
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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