A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920511



Internal ID22695734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96819262..96826493hg38UCSC Ensembl
chr9:99581544..99588775hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg387232
hg197232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448367
Samples
Known GenesZNF782
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920511
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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