A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362022



Internal ID21019575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:175362798..175465883hg38UCSC Ensembl
chr3:175080587..175183671hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38103086
hg19103085
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18098772
Samples
Known GenesMIR4789, MIR548AY, NAALADL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362022
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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