A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363115



Internal ID21020668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119986527..119987404hg38UCSC Ensembl
chr3:119705374..119706251hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38878
hg19878
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093560
Samples
Known GenesGSK3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363115
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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