A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6369n100



Internal ID19016737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:57176322..57960277hg38UCSC Ensembl
chr7:57244029..58019983hg19UCSC Ensembl
chr7:57247971..58023925hg18UCSC Ensembl
Cytoband7p11.1
Allele length
AssemblyAllele length
hg38783956
hg19775955
hg18775955
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1017873, nsv1029476
Samples
Known GenesGUSBP10, MIR3147, ZNF716
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6369n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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