A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368280



Internal ID21025833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:104117531..104266657hg38UCSC Ensembl
chr3:103836375..103985501hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38149127
hg19149127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092323
Samples
Known GenesMIR548A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368280
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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