A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6501n100



Internal ID22792588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76799301..77118682hg38UCSC Ensembl
chr7:76428618..76747999hg19UCSC Ensembl
chr7:76266554..76585935hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38319382
hg19319382
hg18319382
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018360, nsv1035092, nsv1029119, nsv1018899, nsv1019630
Samples
Known GenesDTX2P1-UPK3BP1-PMS2P11, LOC100132832
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6501n100
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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