A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17430366



Internal ID22488236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:90998823..91003673hg38UCSC Ensembl
chr9:93761105..93765955hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg384851
hg194851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5924695
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17430366
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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