A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588062



Internal ID21780105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93800006..93800330hg38UCSC Ensembl
chr11:93533172..93533496hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6040099
Supporting Variants
Samples
Known GenesMED17
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588062
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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