A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521927



Internal ID15449220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:233532980..233534639hg38UCSC Ensembl
Innerchr1:233668726..233670385hg19UCSC Ensembl
Innerchr1:231735349..231737008hg18UCSC Ensembl
Innerchr1:229975461..229977120hg17UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg381660
hg191660
hg181660
hg171660
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694697
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521927
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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