A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17458573



Internal ID22516456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129898550..129941618hg38UCSC Ensembl
chr11:129768445..129811513hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3843069
hg1943069
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866783
Supporting Variants
Samples
Known GenesPRDM10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17458573
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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