A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926073



Internal ID22701300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:7854543..7879633hg38UCSC Ensembl
chr9:7854543..7879633hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3825091
hg1925091
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437055
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926073
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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