A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17030547



Internal ID88077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5788627..5789256hg38UCSC Ensembl
chr10:5830590..5831219hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5490861
Supporting Variants
Samples
Known GenesGDI2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17030547
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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