A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17433701



Internal ID22491571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:82327712..82333219hg38UCSC Ensembl
chr9:84942627..84948134hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg385508
hg195508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5913199
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17433701
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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