A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902433



Internal ID22677592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75532411..75556751hg38UCSC Ensembl
chr6:76242127..76266467hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3824341
hg1924341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448118
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902433
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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