A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046568



Internal ID98856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61628600..61628676hg38UCSC Ensembl
chr11:61396072..61396148hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5495084
Supporting Variants
Samples
Known GenesRPLP0P2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046568
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002029


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