A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026031



Internal ID85087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81918552..81947876hg38UCSC Ensembl
chr9:84533467..84562791hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3829325
hg1929325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142750
Supporting Variants
Samples
Known GenesSPATA31D3, SPATA31D4, SPATA31D5P
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026031
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.006194


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