A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17577594



Internal ID21769637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100073212..100083142hg38UCSC Ensembl
chr9:102835494..102845424hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg389931
hg199931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6011515
Supporting Variants
Samples
Known GenesERP44
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17577594
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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