A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6622n100



Internal ID22792709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:133375782..133433852hg38UCSC Ensembl
chr7:133060536..133118606hg19UCSC Ensembl
chr7:132711076..132769146hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3858071
hg1958071
hg1858071
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018261, nsv1020266
Samples
Known GenesEXOC4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6622n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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