A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17458299



Internal ID22516181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64764464..64765674hg38UCSC Ensembl
chr11:64531936..64533146hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381211
hg191211
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5851498
Supporting Variants
Samples
Known GenesSF1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17458299
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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