A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17579565



Internal ID21771608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64213420..64213420hg38UCSC Ensembl
chr11:63980892..63980892hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6083423
Supporting Variants
Samples
Known GenesFERMT3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17579565
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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