A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv236e55



Internal ID22761186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101289049..101499978hg38UCSC Ensembl
chr7:100932330..101143259hg19UCSC Ensembl
chr7:100719050..100929979hg18UCSC Ensembl
chr7:100525765..100736694hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38210930
hg19210930
hg18210930
hg17210930
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2752136, esv2752137, esv2752135
SamplesSPC_162, BEC_385, BEC_397
Known GenesCOL26A1, RABL5
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)dgv236e55
Frequency
Sample Size771
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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