A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026611



Internal ID85475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104759903..104765468hg38UCSC Ensembl
chr9:107522184..107527749hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg385566
hg195566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5490505
Supporting Variants
Samples
Known GenesNIPSNAP3A, NIPSNAP3B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026611
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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