A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453967



Internal ID21111520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92135754..92136175hg38UCSC Ensembl
chr9:94898036..94898457hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38422
hg19422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194529
Samples
Known GenesLOC100128076
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453967
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