A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6076n100



Internal ID22792163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:81700080..81732560hg38UCSC Ensembl
chr6:82409797..82442277hg19UCSC Ensembl
chr6:82466516..82498996hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3832481
hg1932481
hg1832481
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1032896, nsv1017529, nsv1025966
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)dgv6076n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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