A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367958



Internal ID21025511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150262013..150270960hg38UCSC Ensembl
chr3:149979800..149988747hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg388948
hg198948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096561
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367958
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