A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6242n100



Internal ID20157858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:5813926..5897257hg38UCSC Ensembl
chr7:5853557..5936888hg19UCSC Ensembl
chr7:5820083..5903414hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3883332
hg1983332
hg1883332
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1024555, nsv1030492, nsv1027345, nsv1025720
Samples
Known GenesOCM, ZNF815P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6242n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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