A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362257



Internal ID21019810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:138520235..138891008hg38UCSC Ensembl
chr3:138239077..138609850hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38370774
hg19370774
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093889
Samples
Known GenesCEP70, FAIM, PIK3CB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362257
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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