A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521773



Internal ID15449066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:89667023..89677669hg38UCSC Ensembl
Innerchr1:90132582..90143228hg19UCSC Ensembl
Innerchr1:89905170..89915816hg18UCSC Ensembl
Innerchr1:89844603..89855249hg17UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3810647
hg1910647
hg1810647
hg1710647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694540
Samples
Known GenesLRRC8C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521773
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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