A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6466n100



Internal ID20158082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73245562..73420814hg38UCSC Ensembl
chr7:72659595..72835144hg19UCSC Ensembl
chr7:72297531..72473080hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38175253
hg19175550
hg18175550
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019798, nsv1032536
Samples
Known GenesFKBP6, NSUN5, TRIM50
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6466n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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