A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524986



Internal ID15452279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12518619..12518833hg38UCSC Ensembl
Innerchr16:12612476..12612690hg19UCSC Ensembl
Innerchr16:12519977..12520191hg18UCSC Ensembl
Innerchr16:12519977..12520191hg17UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38215
hg19215
hg18215
hg17215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701015
Samples
Known GenesSNX29
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524986
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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