A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032413



Internal ID89304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9449108..9454535hg38UCSC Ensembl
chr10:9491071..9496498hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg385428
hg195428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5483359
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032413
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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