A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369652



Internal ID21027205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18036094..18036824hg38UCSC Ensembl
chr3:18077586..18078316hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100460
Samples
Known GenesLOC339862
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369652
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