A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17041797



Internal ID95568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7540405..7638702hg38UCSC Ensembl
chr11:7561636..7659933hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3898298
hg1998298
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5504023
Supporting Variants
Samples
Known GenesPPFIBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17041797
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000625


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