A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352402



Internal ID22578071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59127677..59133064hg38UCSC Ensembl
chr11:58895150..58900537hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg385388
hg195388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5923295
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352402
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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