A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442007



Internal ID21099560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:102020558..102141301hg38UCSC Ensembl
chr9:104782840..104903583hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38120744
hg19120744
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18172540
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442007
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