A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605085



Internal ID20978156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149618250..149625798hg38UCSC Ensembl
chr6:149939386..149946934hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg387549
hg197549
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217089
Samples
Known GenesKATNA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605085
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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