A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316460



Internal ID20849539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40943827..40947806hg38UCSC Ensembl
chr1:41409499..41413478hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg383980
hg193980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060785
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316460
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