A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361580



Internal ID21019133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61391829..61401665hg38UCSC Ensembl
chr3:61377503..61387339hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg389837
hg199837
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101705
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361580
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