A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6301n223



Internal ID22809269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85832201..85862900hg38UCSC Ensembl
chr6:86541919..86572618hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3830700
hg1930700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6414413, nsv6405025, nsv6396676, nsv6411513
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6301n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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