A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519366



Internal ID15099973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1851210..1961125hg38UCSC Ensembl
Innerchr16:1901211..2011126hg19UCSC Ensembl
Innerchr16:1841212..1951127hg18UCSC Ensembl
Innerchr16:1841212..1951127hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38109916
hg19109916
hg18109916
hg17109916
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696813
Samples
Known GenesHS3ST6, LINC00254, MEIOB, MSRB1, NDUFB10, RPL3L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519366
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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