A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17035883



Internal ID91664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:60240054..60240067hg38UCSC Ensembl
chr10:61999812..61999825hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5547927
Supporting Variants
Samples
Known GenesANK3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17035883
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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