A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17461551



Internal ID22519436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:123661386..123667923hg38UCSC Ensembl
chr11:123532094..123538631hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg386538
hg196538
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860052
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17461551
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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