A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516019



Internal ID15443076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:75432798..75439434hg38UCSC Ensembl
Innerchr16:75466696..75473332hg19UCSC Ensembl
Innerchr16:74024197..74030833hg18UCSC Ensembl
Innerchr16:74024197..74030833hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg386637
hg196637
hg186637
hg176637
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv671569, nssv687105, nssv660559, nssv657988, nssv693493, nssv668952, nssv671442, nssv683339, nssv665764, nssv690364, nssv669011, nssv692119
Samples
Known GenesCFDP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516019
Frequency
Sample Size2026
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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