A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608055



Internal ID20981126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:148307322..148333517hg38UCSC Ensembl
chr6:148628458..148654653hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3826196
hg1926196
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217074
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608055
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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