A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413599



Internal ID21071152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:80877413..81564382hg38UCSC Ensembl
chr6:81587130..82274099hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38686970
hg19686970
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230378
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413599
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer