A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374247



Internal ID21031800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:40022273..40022790hg38UCSC Ensembl
chr3:40063764..40064281hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38518
hg19518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100919
Samples
Known GenesMYRIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374247
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