A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213065



Internal ID20780105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:142315534..142318126hg38UCSC Ensembl
chr4:143236687..143239279hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg382593
hg192593
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6377271
Supporting Variants
Samples
Known GenesINPP4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213065
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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