A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17454045



Internal ID22511920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125908163..125909974hg38UCSC Ensembl
chr11:125778058..125779869hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg381812
hg191812
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5850900
Supporting Variants
Samples
Known GenesDDX25
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17454045
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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