A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444522



Internal ID21102075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86042050..86044832hg38UCSC Ensembl
chr9:88656965..88659747hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg382783
hg192783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181643
Samples
Known GenesGOLM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444522
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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