A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611122



Internal ID20984193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:121791170..121840977hg38UCSC Ensembl
chr6:122112316..122162123hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3849808
hg1949808
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214589
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611122
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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