A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6379n100



Internal ID22792466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:57720893..57960277hg38UCSC Ensembl
chr7:57780599..58019983hg19UCSC Ensembl
chr7:57784541..58023925hg18UCSC Ensembl
Cytoband7p11.1
Allele length
AssemblyAllele length
hg38239385
hg19239385
hg18239385
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1016501, nsv1016244
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6379n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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