A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522255



Internal ID15449548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:175858547..175880762hg38UCSC Ensembl
Innerchr1:175827683..175849898hg19UCSC Ensembl
Innerchr1:174094306..174116521hg18UCSC Ensembl
Innerchr1:172559340..172581555hg17UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg3822216
hg1922216
hg1822216
hg1722216
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695035
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522255
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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