A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606696



Internal ID20979767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99414864..99441267hg38UCSC Ensembl
chr6:99862740..99889143hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg3826404
hg1926404
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219887
Samples
Known GenesPNISR, USP45
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606696
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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