A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522935



Internal ID15103542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:70421500..70422418hg38UCSC Ensembl
Innerchr1:70887183..70888101hg19UCSC Ensembl
Innerchr1:70659771..70660689hg18UCSC Ensembl
Innerchr1:70599204..70600122hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38919
hg19919
hg18919
hg17919
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698598
Samples
Known GenesCTH
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522935
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer