A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6636n100



Internal ID22792723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134530651..134579534hg38UCSC Ensembl
chr7:134215403..134264286hg19UCSC Ensembl
chr7:133865943..133914826hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3848884
hg1948884
hg1848884
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033587, nsv1027442, nsv1023962, nsv1033209, nsv1034066
Samples
Known GenesAKR1B10, AKR1B15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6636n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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