A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16902058



Internal ID2168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37725880..37726045hg38UCSC Ensembl
chr1:38191552..38191717hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5427587
Supporting Variants
Samples
Known GenesEPHA10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16902058
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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