A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17580789



Internal ID21772832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7534365..7534365hg38UCSC Ensembl
chr11:7555596..7555596hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382502
hg192502
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6080673
Supporting Variants
Samples
Known GenesPPFIBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17580789
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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