A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373159



Internal ID21030712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:138098365..138099695hg38UCSC Ensembl
chr3:137817207..137818537hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg381331
hg191331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093874
Samples
Known GenesDZIP1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373159
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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