A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6511n100



Internal ID22792598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:79172440..79227321hg38UCSC Ensembl
chr7:78801756..78856637hg19UCSC Ensembl
chr7:78639692..78694573hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3854882
hg1954882
hg1854882
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1020756, nsv1015177, nsv1027497, nsv1019480, nsv1021266, nsv1032357, nsv1028020, nsv1032979, nsv1029701
Samples
Known GenesMAGI2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6511n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss59
Observed Complex0
Frequencyn/a


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