A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617689



Internal ID20990760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108001618..108003572hg38UCSC Ensembl
chr6:108322822..108324776hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381955
hg191955
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216780
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617689
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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