A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518855



Internal ID15099462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:77950984..77990671hg38UCSC Ensembl
Innerchr1:78416669..78456355hg19UCSC Ensembl
Innerchr1:78189257..78228943hg18UCSC Ensembl
Innerchr1:78128690..78168376hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3839688
hg1939687
hg1839687
hg1739687
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694281
Samples
Known GenesFUBP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518855
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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