A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035881



Internal ID91663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:60236243..60236419hg38UCSC Ensembl
chr10:61996001..61996177hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474308
Supporting Variants
Samples
Known GenesANK3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035881
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.008742


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