A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919968



Internal ID22695191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137424503..137425448hg38UCSC Ensembl
chr9:140318955..140319900hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38946
hg19946
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429658
Samples
Known GenesNOXA1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919968
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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