A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522422



Internal ID15103029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37873431..37898917hg38UCSC Ensembl
Innerchr3:37914922..37940408hg19UCSC Ensembl
Innerchr3:37889926..37915412hg18UCSC Ensembl
Innerchr3:37889926..37915412hg17UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3825487
hg1925487
hg1825487
hg1725487
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705775
Samples
Known GenesCTDSPL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522422
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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