A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702660



Internal ID15092626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82687819..82692879hg38UCSC Ensembl
Innerchr16:82721424..82726484hg19UCSC Ensembl
Innerchr16:81278925..81283985hg18UCSC Ensembl
Innerchr16:81278925..81283985hg17UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg385061
hg195061
hg185061
hg175061
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526366
Supporting Variants
Samples
Known GenesCDH13, MIR8058
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702660
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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