A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6429n100



Internal ID22792516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:62720720..63332411hg38UCSC Ensembl
chr7:62181098..62792789hg19UCSC Ensembl
chr7:61818533..62430224hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38611692
hg19611692
hg18611692
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1030758, nsv1027893, nsv1034302
Samples
Known GenesZNF733P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6429n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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