A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331443



Internal ID20864606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:243984396..243985158hg38UCSC Ensembl
chr1:244147698..244148460hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38763
hg19763
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059610
Samples
Known GenesLOC339529
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331443
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