A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035472



Internal ID91391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:64939092..64962909hg38UCSC Ensembl
chr10:66698850..66722667hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3823818
hg1923818
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557431
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035472
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000937


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