A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv103n21



Internal ID18990576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:132117051..132442096hg38UCSC Ensembl
chr12:132601596..133018682hg19UCSC Ensembl
chr12:131167549..131528755hg18UCSC Ensembl
chr12:131267826..131629032hg17UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38325046
hg19417087
hg18361207
hg17361207
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv527956, nsv518033
Samples
Known GenesDDX51, EP400NL, GALNT9, LOC100130238, NOC4L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv103n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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