A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6726n100



Internal ID22792813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:144164657..144377836hg38UCSC Ensembl
chr7:143861750..144074929hg19UCSC Ensembl
chr7:143492683..143705862hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38213180
hg19213180
hg18213180
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1027374, nsv1027780, nsv1028852, nsv1026730, nsv1023169, nsv1032530
Samples
Known GenesARHGEF34P, ARHGEF35, ARHGEF5, CTAGE4, CTAGE8, OR2A1, OR2A20P, OR2A42, OR2A7, OR2A9P, RNU6-57P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6726n100
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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