A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17037002



Internal ID92422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74099318..74099897hg38UCSC Ensembl
chr10:75859076..75859655hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38580
hg19580
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5481105
Supporting Variants
Samples
Known GenesVCL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17037002
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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