A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605954



Internal ID20979025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:126536792..126537581hg38UCSC Ensembl
chr6:126857938..126858727hg19UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg38790
hg19790
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138764
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605954
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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