A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6529n100



Internal ID22792616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:89902753..90267449hg38UCSC Ensembl
chr7:89532067..89896763hg19UCSC Ensembl
chr7:89370003..89734699hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38364697
hg19364697
hg18364697
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026427, nsv1018968
Samples
Known GenesC7orf63, DPY19L2P4, STEAP1, STEAP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6529n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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