A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377398



Internal ID21034951
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 StatusM
Merged Variants
Supporting Variantsnssv18109458
Samples
Known GenesPABPC4L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377398
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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