A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375273



Internal ID21032826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:181462101..181463300hg38UCSC Ensembl
chr3:181179889..181181088hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097789
Samples
Known GenesSOX2-OT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375273
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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