A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361838



Internal ID21019391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:181659839..181660920hg38UCSC Ensembl
chr3:181377627..181378708hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg381082
hg191082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097802
Samples
Known GenesSOX2-OT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361838
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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