A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606934



Internal ID20980005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:122110711..122112798hg38UCSC Ensembl
chr6:122431857..122433944hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg382088
hg192088
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137337
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606934
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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