A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032300



Internal ID89235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26505692..26505768hg38UCSC Ensembl
chr10:26794621..26794697hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492099
Supporting Variants
Samples
Known GenesAPBB1IP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032300
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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