A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923096



Internal ID22698322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79299929..79299990hg38UCSC Ensembl
chr10:81059686..81059747hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358653
Samples
Known GenesZMIZ1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923096
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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