A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17354532



Internal ID22580201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34489219..34491549hg38UCSC Ensembl
chr11:34510766..34513096hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg382331
hg192331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5924155
Supporting Variants
Samples
Known GenesELF5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17354532
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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