A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404029



Internal ID21061582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41267256..41270995hg38UCSC Ensembl
chr6:41234994..41238733hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg383740
hg193740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143322
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404029
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