A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606533



Internal ID20979604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132736590..132759774hg38UCSC Ensembl
chr6:133057729..133080913hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3823185
hg1923185
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215585
Samples
Known GenesVNN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606533
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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