A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17040791



Internal ID94908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118321860..118325315hg38UCSC Ensembl
chr10:120081372..120084827hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg383456
hg193456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5499316
Supporting Variants
Samples
Known GenesFAM204A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17040791
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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