A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526077



Internal ID15106684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:123181245..123245232hg38UCSC Ensembl
Innerchr3:122900092..122964079hg19UCSC Ensembl
Innerchr3:124382782..124446769hg18UCSC Ensembl
Innerchr3:124382782..124446769hg17UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg3863988
hg1963988
hg1863988
hg1763988
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv297n21
Supporting Variantsnssv702319
Samples
Known GenesSEC22A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526077
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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