A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527197



Internal ID15107804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11977484..11979943hg38UCSC Ensembl
Innerchr16:12071341..12073800hg19UCSC Ensembl
Innerchr16:11978842..11981301hg18UCSC Ensembl
Innerchr16:11978842..11981301hg17UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg382460
hg192460
hg182460
hg172460
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703596
Samples
Known GenesSNX29
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527197
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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