A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915033



Internal ID22690251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131822325..131822425hg38UCSC Ensembl
chr9:134697712..134697812hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445335
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915033
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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