A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612686



Internal ID20985757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:104432560..104507145hg38UCSC Ensembl
chr6:104880435..104955020hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3874586
hg1974586
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216533
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612686
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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