A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292757



Internal ID20501975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:14955095..14955095hg38UCSC Ensembl
chr4:14956719..14956719hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg382983
hg192983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4757038
Supporting Variants
Samples
Known GenesCPEB2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292757
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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