A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17542082



Internal ID21866437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56733590..56751809hg38UCSC Ensembl
chr4:57599756..57617975hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3818220
hg1918220
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5997752
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17542082
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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