A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456923



Internal ID22514803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47219363..47220612hg38UCSC Ensembl
chr11:47240914..47242163hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381250
hg191250
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5860411
Supporting Variants
Samples
Known GenesDDB2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456923
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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