A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17354220



Internal ID22579889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:54547778..54551351hg38UCSC Ensembl
chr11:51567929..51571502hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg383574
hg193574
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5920333
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17354220
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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