A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413587



Internal ID21071140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:81822680..81823232hg38UCSC Ensembl
chr6:82532397..82532949hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38553
hg19553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18144603
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413587
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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