A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328842



Internal ID20861992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67472419..67474663hg38UCSC Ensembl
chr1:67938102..67940346hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg382245
hg192245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062666
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328842
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