A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17353193



Internal ID22578862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125815104..125910636hg38UCSC Ensembl
chr11:125684999..125780531hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3895533
hg1995533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5911765
Supporting Variants
Samples
Known GenesDDX25, HYLS1, PATE4, PUS3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17353193
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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