A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404074



Internal ID21061627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4109780..4110312hg38UCSC Ensembl
chr6:4110014..4110546hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143313
Samples
Known GenesC6orf201
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404074
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