A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17036371



Internal ID91995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88881415..88881560hg38UCSC Ensembl
chr10:90641172..90641317hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488845
Supporting Variants
Samples
Known GenesSTAMBPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17036371
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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