A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611590



Internal ID20984661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116696601..116699900hg38UCSC Ensembl
chr6:117017764..117021063hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6374n223
Supporting Variantsnssv18137166
Samples
Known GenesKPNA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611590
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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