A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv252n97



Internal ID22815649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:76712780..76758214hg38UCSC Ensembl
chr6:77422497..77467931hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3845435
hg1945435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1156537, nsv1156538, nsv1156536
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv252n97
Frequency
Sample Size131
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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