A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17037611



Internal ID92827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97431320..97431444hg38UCSC Ensembl
chr10:99191077..99191201hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5490345
Supporting Variants
Samples
Known GenesPGAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17037611
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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