A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6727n100



Internal ID20158343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:144164657..144409403hg38UCSC Ensembl
chr7:143861750..144106496hg19UCSC Ensembl
chr7:143492683..143737429hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38244747
hg19244747
hg18244747
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019408, nsv1016085, nsv1016605, nsv1018297, nsv1034764, nsv1015714, nsv1020823
Samples
Known GenesARHGEF34P, ARHGEF35, ARHGEF5, CTAGE4, CTAGE8, NOBOX, 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)dgv6727n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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