A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525605



Internal ID15452898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:87450232..87454579hg38UCSC Ensembl
Innerchr16:87483838..87488185hg19UCSC Ensembl
Innerchr16:86041339..86045686hg18UCSC Ensembl
Innerchr16:86041339..86045686hg17UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg384348
hg194348
hg184348
hg174348
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701749
Samples
Known GenesZCCHC14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525605
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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