A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035425



Internal ID91357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:58681437..58681488hg38UCSC Ensembl
chr10:60441197..60441248hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5405588
Supporting Variants
Samples
Known GenesBICC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035425
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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