A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6136n100



Internal ID22792223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110063851..110095665hg38UCSC Ensembl
chr6:110385054..110416868hg19UCSC Ensembl
chr6:110491747..110523561hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3831815
hg1931815
hg1831815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1017551, nsv1029169, nsv1023185
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)dgv6136n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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