A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365014



Internal ID21022567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139112229..139112856hg38UCSC Ensembl
chr3:138831071..138831698hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38628
hg19628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093927
Samples
Known GenesBPESC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365014
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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