A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327687



Internal ID20860828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8902653..8919435hg38UCSC Ensembl
chr1:8962712..8979494hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3816783
hg1916783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064905
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327687
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