A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6111n100



Internal ID22792198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:98099939..98204719hg38UCSC Ensembl
chr6:98547815..98652595hg19UCSC Ensembl
chr6:98654536..98759316hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38104781
hg19104781
hg18104781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1029201, nsv1024708
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)dgv6111n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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