A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17049774



Internal ID101077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:88593827..88594020hg38UCSC Ensembl
chr11:88326995..88327188hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5501053
Supporting Variants
Samples
Known GenesGRM5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17049774
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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