A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370752



Internal ID21028305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42847151..42857333hg38UCSC Ensembl
chr3:42888643..42898825hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3810183
hg1910183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099928
Samples
Known GenesACKR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370752
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