A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925504



Internal ID22700731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14592614..14598817hg38UCSC Ensembl
chr9:14592612..14598815hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg386204
hg196204
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447848
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925504
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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