A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526331



Internal ID15453624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81533949..81534087hg38UCSC Ensembl
Innerchr16:81567554..81567692hg19UCSC Ensembl
Innerchr16:80125055..80125193hg18UCSC Ensembl
Innerchr16:80125055..80125193hg17UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg38139
hg19139
hg18139
hg17139
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702621
Samples
Known GenesCMIP, MIR7854
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526331
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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