A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703263



Internal ID15093229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:451362..810673hg38UCSC Ensembl
Innerchr16:501362..860673hg19UCSC Ensembl
Innerchr16:441363..800674hg18UCSC Ensembl
Innerchr16:441363..800674hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38359312
hg19359312
hg18359312
hg17359312
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526903
Supporting Variants
Samples
Known GenesC16orf11, C16orf13, CAPN15, CCDC78, CHTF18, FAM173A, FAM195A, FBXL16, GNG13, HAGHL, JMJD8, LINC00235, METRN, MIR3176, MIR5587, MIR662, MSLN, NARFL, NHLRC4, PIGQ, PRR25, RAB11FIP3, RAB40C, RHBDL1, RHOT2, RPUSD1, STUB1, WDR24, WDR90, WFIKKN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703263
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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