A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358705



Internal ID21016258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25874642..25923483hg38UCSC Ensembl
chr3:25916133..25964974hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3848842
hg1948842
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101148
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358705
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