A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613901



Internal ID20986972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:135356711..135667377hg38UCSC Ensembl
chr6:135677849..135988515hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38310667
hg19310667
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215619
Samples
Known GenesAHI1, LINC00271
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613901
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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