A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6201n100



Internal ID22792288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168787034..168822314hg38UCSC Ensembl
chr6:169187129..169222409hg19UCSC Ensembl
chr6:168929054..168964334hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3835281
hg1935281
hg1835281
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1021422, nsv1033784, nsv1017508, nsv1031735
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)dgv6201n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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