A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033106



Internal ID89767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35851588..35870213hg38UCSC Ensembl
chr10:36140516..36159141hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3818626
hg1918626
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555354
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033106
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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