A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17584223



Internal ID21776266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91827600..91827774hg38UCSC Ensembl
chr9:94589882..94590056hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6009579
Supporting Variants
Samples
Known GenesROR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17584223
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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