A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604351



Internal ID20977422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113532166..113541942hg38UCSC Ensembl
chr6:113853368..113863144hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg389777
hg199777
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137073
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604351
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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