A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038511



Internal ID93406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:75536430..75537942hg38UCSC Ensembl
chr10:77296188..77297700hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg381513
hg191513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5493573
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038511
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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