A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11685n54



Internal ID22779580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:144280907..144377836hg38UCSC Ensembl
chr7:143978000..144074929hg19UCSC Ensembl
chr7:143608933..143705862hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3896930
hg1996930
hg1896930
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv608854, nsv608852, nsv608851
Samples
Known GenesARHGEF34P, ARHGEF5, OR2A1, OR2A20P, OR2A42, OR2A9P, RNU6-57P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11685n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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