A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032299



Internal ID89234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26505427..26505516hg38UCSC Ensembl
chr10:26794356..26794445hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486952
Supporting Variants
Samples
Known GenesAPBB1IP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032299
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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