A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv272n97



Internal ID22815669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:144176859..144378425hg38UCSC Ensembl
chr7:143873952..144075518hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38201567
hg19201567
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1156752, nsv1156748, nsv1156750, nsv1156747, nsv1156751
Samples
Known GenesARHGEF34P, ARHGEF35, ARHGEF5, CTAGE4, CTAGE8, OR2A1, OR2A20P, OR2A42, OR2A7, OR2A9P, RNU6-57P
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv272n97
Frequency
Sample Size131
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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