A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6518n100



Internal ID22792605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:83763785..83877327hg38UCSC Ensembl
chr7:83393101..83506643hg19UCSC Ensembl
chr7:83231037..83344579hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38113543
hg19113543
hg18113543
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1017260, nsv1020865
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)dgv6518n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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