A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600829



Internal ID20973900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111074401..111078918hg38UCSC Ensembl
chr6:111395604..111400121hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384518
hg194518
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216814
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600829
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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