A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518052



Internal ID15098659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:120174410..120177810hg38UCSC Ensembl
Innerchr3:119893257..119896657hg19UCSC Ensembl
Innerchr3:121375947..121379347hg18UCSC Ensembl
Innerchr3:121375947..121379347hg17UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg383401
hg193401
hg183401
hg173401
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695463
Samples
Known GenesGPR156
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518052
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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