A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17037603



Internal ID92822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97398034..97398353hg38UCSC Ensembl
chr10:99157791..99158110hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5475902
Supporting Variants
Samples
Known GenesRRP12
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17037603
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.273267


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