A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039782



Internal ID94242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97699971..97700257hg38UCSC Ensembl
chr10:99459728..99460014hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38287
hg19287
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147465
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039782
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.043553


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