A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403363



Internal ID21060916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:76586701..76589500hg38UCSC Ensembl
chr6:77296418..77299217hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6274n223
Supporting Variantsnssv18148208
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403363
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