A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17451380



Internal ID22509252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128219529..128230062hg38UCSC Ensembl
chr11:128089424..128099957hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3810534
hg1910534
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848436
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17451380
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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