A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17361350



Internal ID22587019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72881879..72882179hg38UCSC Ensembl
chr11:72592924..72593224hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5921827
Supporting Variants
Samples
Known GenesFCHSD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17361350
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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