A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386669



Internal ID21044222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:75925737..75926333hg38UCSC Ensembl
chr4:76846890..76847486hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38597
hg19597
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120239
Samples
Known GenesNAAA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386669
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