A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521875



Internal ID15449168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81477137..81481145hg38UCSC Ensembl
Innerchr16:81510742..81514750hg19UCSC Ensembl
Innerchr16:80068243..80072251hg18UCSC Ensembl
Innerchr16:80068243..80072251hg17UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg384009
hg194009
hg184009
hg174009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694646
Samples
Known GenesCMIP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521875
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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