A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397798



Internal ID21055351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:70658797..70667526hg38UCSC Ensembl
chr6:71368500..71377229hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg388730
hg198730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18144457
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397798
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