A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372459



Internal ID21030012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13673901..13677500hg38UCSC Ensembl
chr3:13715401..13718999hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg383600
hg193599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094958
Samples
Known GenesLINC00620
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372459
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