A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616014



Internal ID20989085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132912284..133124144hg38UCSC Ensembl
chr6:133233423..133445283hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38211861
hg19211861
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215587
Samples
Known GenesLINC00326
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616014
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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