A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6166n100



Internal ID22792253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160603885..160648356hg38UCSC Ensembl
chr6:161024917..161069388hg19UCSC Ensembl
chr6:160944907..160989378hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3844472
hg1944472
hg1844472
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1021138, nsv1034147, nsv1030067, nsv1019635, nsv1017965, nsv1025879, nsv1020754, nsv1018420, nsv1033987, nsv1030890, nsv1028593, nsv1022363
Samples
Known GenesLPA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6166n100
Frequency
Sample Size11257
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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