A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6365n100



Internal ID22792452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:56718140..56800076hg38UCSC Ensembl
chr7:56785833..56867769hg19UCSC Ensembl
chr7:56753327..56835263hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3881937
hg1981937
hg1881937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1025582, nsv1015445
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)dgv6365n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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