A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6221n100



Internal ID22792308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:3085878..3168438hg38UCSC Ensembl
chr7:3125512..3208071hg19UCSC Ensembl
chr7:3092038..3174597hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3882561
hg1982560
hg1882560
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1027945, nsv1020680
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)dgv6221n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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