A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526215



Internal ID15106822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:199889..203266hg38UCSC Ensembl
Innerchr3:241572..244949hg19UCSC Ensembl
Innerchr3:216572..219949hg18UCSC Ensembl
Innerchr3:216572..219949hg17UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg383378
hg193378
hg183378
hg173378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv266n21
Supporting Variantsnssv702479
Samples
Known GenesCHL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526215
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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