A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1041n145



Internal ID22814057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:61525615..61542466hg38UCSC Ensembl
chr6:62235520..62252371hg19UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg3816852
hg1916852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3116993, nsv3111901
Samplessample412, sample360
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1041n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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