A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527809



Internal ID15455102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:224858126..224861045hg38UCSC Ensembl
Innerchr1:225045828..225048747hg19UCSC Ensembl
Innerchr1:223112451..223115370hg18UCSC Ensembl
Innerchr1:221352563..221355482hg17UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg382920
hg192920
hg182920
hg172920
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704303
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527809
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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