A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704939



Internal ID15441591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:451362..605686hg38UCSC Ensembl
Innerchr16:501362..655686hg19UCSC Ensembl
Innerchr16:441363..595687hg18UCSC Ensembl
Innerchr16:441363..595687hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38154325
hg19154325
hg18154325
hg17154325
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528354
Supporting Variants
Samples
Known GenesC16orf11, CAPN15, LINC00235, MIR3176, MIR5587, NHLRC4, PIGQ, RAB11FIP3, RAB40C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704939
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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