A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6701n100



Internal ID22792788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143514550..143795264hg38UCSC Ensembl
chr7:143211643..143492357hg19UCSC Ensembl
chr7:142921765..143123290hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38280715
hg19280715
hg18201526
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018685, nsv1032597, nsv1019171, nsv1018097, nsv1030894, nsv1029083, nsv1019237
Samples
Known GenesCTAGE15, CTAGE6, EPHA1-AS1, FAM115C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6701n100
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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