A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035344



Internal ID91302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78173134..78177058hg38UCSC Ensembl
chr10:79932891..79936815hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg383925
hg193925
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492466
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035344
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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