A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411513



Internal ID21069066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85833401..85862900hg38UCSC Ensembl
chr6:86543119..86572618hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3829500
hg1929500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6301n223
Supporting Variantsnssv18146078
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411513
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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