A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6391n100



Internal ID22792478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:61272656..62978903hg38UCSC Ensembl
chr7:61255381..62439281hg19UCSC Ensembl
chr7:61259323..62076716hg18UCSC Ensembl
Cytoband7q11.1
Allele length
AssemblyAllele length
hg381706248
hg191183901
hg18817394
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034234, nsv1028195, nsv1028743
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)dgv6391n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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