A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356542



Internal ID21014095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:171189410..171190032hg38UCSC Ensembl
chr3:170907199..170907821hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38623
hg19623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097193
Samples
Known GenesTNIK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356542
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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