A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18109458



Internal ID20676498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:134060021..134378013hg38UCSC Ensembl
chr4:134981176..135299168hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38317993
hg19317993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6377398
Supporting Variants
Samples
Known GenesPABPC4L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18109458
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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