A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360893



Internal ID21018446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:86600340..86625155hg38UCSC Ensembl
chr3:86649490..86674305hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3824816
hg1924816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103973
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360893
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