A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702621



Internal ID15439273
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526331
Supporting Variants
Samples
Known GenesCMIP, MIR7854
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702621
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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