A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17446728



Internal ID22504598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:25916061..25988079hg38UCSC Ensembl
chr9:25916059..25988077hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3872019
hg1972019
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5920539
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17446728
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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