A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17597182



Internal ID21789225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96349320..96349519hg38UCSC Ensembl
chr9:99111602..99111801hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6013973
Supporting Variants
Samples
Known GenesSLC35D2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17597182
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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