A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524025



Internal ID15451318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11915924..11923062hg38UCSC Ensembl
Innerchr16:12009781..12016919hg19UCSC Ensembl
Innerchr16:11917282..11924420hg18UCSC Ensembl
Innerchr16:11917282..11924420hg17UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg387139
hg197139
hg187139
hg177139
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699887
Samples
Known GenesGSPT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524025
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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