A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6468n100



Internal ID22792555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75701432..75777782hg38UCSC Ensembl
chr7:75330750..75407100hg19UCSC Ensembl
chr7:75168686..75245036hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3876351
hg1976351
hg1876351
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1027242, nsv1017751
Samples
Known GenesCCL26, HIP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6468n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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