A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17040867



Internal ID94963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119183896..119191538hg38UCSC Ensembl
chr10:120943408..120951050hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg387643
hg197643
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563211
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17040867
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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