A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326672



Internal ID20859809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86931301..86931880hg38UCSC Ensembl
chr1:87396984..87397563hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38580
hg19580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064469
Samples
Known GenesHS2ST1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326672
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