A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6702n100



Internal ID19017070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143514550..143850167hg38UCSC Ensembl
chr7:143211643..143547260hg19UCSC Ensembl
chr7:142921765..143178193hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38335618
hg19335618
hg18256429
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034914, nsv1027295, nsv1025356, nsv1017608, nsv1023216, nsv1016132, nsv1022857, nsv1023551, nsv1017306, nsv1027979, nsv1025340, nsv1016718, nsv1023087, nsv1022365, nsv1017807, nsv1030200, nsv1026280, nsv1032606, nsv1031955, nsv1025503, nsv1031587, nsv1021663, nsv1028268, nsv1019429, nsv1028960, nsv1017445, nsv1029826, nsv1028295, nsv1030809, nsv1031448, nsv1031359, nsv1018780, nsv1024495, nsv1015603, nsv1027657, nsv1033811, nsv1024013, nsv1026541, nsv1021295, nsv1024501, nsv1019550, nsv1023780, nsv1028999, nsv1033726, nsv1022958
Samples
Known GenesCTAGE15, CTAGE6, EPHA1-AS1, FAM115C, LOC154761
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6702n100
Frequency
Sample Size29084
Observed Gain147
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer