A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17556763



Internal ID21881118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:118880986..118880986hg38UCSC Ensembl
chr4:119802141..119802141hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6070908
Supporting Variants
Samples
Known GenesSYNPO2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17556763
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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