A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326995



Internal ID20860132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8950063..8952160hg38UCSC Ensembl
chr1:9010122..9012219hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg382098
hg192098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064927
Samples
Known GenesCA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326995
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