A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039671



Internal ID94166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111787464..111812103hg38UCSC Ensembl
chr10:113547222..113571861hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3824640
hg1924640
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561095
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039671
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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