A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17461630



Internal ID22519515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83497809..83502069hg38UCSC Ensembl
chr11:83208852..83213112hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg384261
hg194261
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855970
Supporting Variants
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17461630
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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