A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6456n100



Internal ID20158072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:71568840..71823976hg38UCSC Ensembl
chr7:71033825..71288961hg19UCSC Ensembl
chr7:70671761..70926897hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38255137
hg19255137
hg18255137
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1024288, nsv1034811, nsv1016182
Samples
Known GenesCALN1, WBSCR17
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6456n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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