A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6532n100



Internal ID22792619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90475310..90538525hg38UCSC Ensembl
chr7:90104624..90167839hg19UCSC Ensembl
chr7:89942560..90005775hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3863216
hg1963216
hg1863216
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1017515, nsv1025620, nsv1030873, nsv1027880
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)dgv6532n100
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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