A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17455875



Internal ID22513752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121828618..121830845hg38UCSC Ensembl
chr11:121699326..121701553hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg382228
hg192228
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5864147
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17455875
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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