A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6258n100



Internal ID22792345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:8839730..9023654hg38UCSC Ensembl
chr7:8879360..9063284hg19UCSC Ensembl
chr7:8845885..9029809hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38183925
hg19183925
hg18183925
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033429, nsv1015951
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)dgv6258n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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