A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528254



Internal ID15455547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:37338411..37352354hg38UCSC Ensembl
Innerchr22:37734452..37748394hg19UCSC Ensembl
Innerchr22:36064398..36078340hg18UCSC Ensembl
Innerchr22:36058952..36072894hg17UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3813944
hg1913943
hg1813943
hg1713943
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704820
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528254
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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