A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035299



Internal ID91268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72075224..72085217hg38UCSC Ensembl
chr10:73834982..73844975hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg389994
hg199994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5487444
Supporting Variants
Samples
Known GenesSPOCK2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035299
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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