A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6638n100



Internal ID22792725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:136208754..136301340hg38UCSC Ensembl
chr7:135893502..135986088hg19UCSC Ensembl
chr7:135544042..135636628hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3892587
hg1992587
hg1892587
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033206, nsv1034145, nsv1025030, nsv1018084
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)dgv6638n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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