A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358242



Internal ID21015795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:126165292..126165635hg38UCSC Ensembl
chr3:125884135..125884478hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094045
Samples
Known GenesALDH1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358242
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