A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6700n100



Internal ID22792787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143512758..143881082hg38UCSC Ensembl
chr7:143209851..143578175hg19UCSC Ensembl
chr7:142919973..143209108hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38368325
hg19368325
hg18289136
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022413, nsv1028235, nsv1017173, nsv1034371, nsv1024714, nsv1015674, nsv1028097, nsv1017304
Samples
Known GenesCTAGE15, CTAGE6, EPHA1-AS1, FAM115A, 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)dgv6700n100
Frequency
Sample Size11257
Observed Gain25
Observed Loss0
Observed Complex0
Frequencyn/a


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