A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17358953



Internal ID22584622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64416030..64416145hg38UCSC Ensembl
chr11:64183502..64183617hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5926708
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17358953
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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