A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409780



Internal ID21067333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:94744856..94925610hg38UCSC Ensembl
chr6:95454574..95635328hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38180755
hg19180755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6321n223
Supporting Variantsnssv18146268
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409780
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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