A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17356536



Internal ID22582205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101423805..101431569hg38UCSC Ensembl
chr11:101294536..101302300hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg387765
hg197765
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918636
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17356536
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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