A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6138n100



Internal ID22792225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113382365..113478754hg38UCSC Ensembl
chr6:113703567..113799956hg19UCSC Ensembl
chr6:113810260..113906649hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3896390
hg1996390
hg1896390
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034256, nsv1021815
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)dgv6138n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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