A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360537



Internal ID21018090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36924944..36970028hg38UCSC Ensembl
chr3:36966435..37011519hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3845085
hg1945085
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099129
Samples
Known GenesTRANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360537
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