A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6101n100



Internal ID22792188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:94746243..94934177hg38UCSC Ensembl
chr6:95455961..95643895hg19UCSC Ensembl
chr6:95512682..95700616hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38187935
hg19187935
hg18187935
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1029987, nsv1028225
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)dgv6101n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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