A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399454



Internal ID21057007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25135836..25318733hg38UCSC Ensembl
chr6:25136064..25318961hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38182898
hg19182898
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235677
Samples
Known GenesCMAHP, LRRC16A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399454
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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