A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375826



Internal ID21033379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:150287337..150292952hg38UCSC Ensembl
chr4:151208489..151214104hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg385616
hg195616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18112259
Samples
Known GenesLRBA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375826
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