A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3944425



Internal ID21364494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3310321..3310380hg38UCSC Ensembl
chr6:3310555..3310614hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15197005
SamplesHG002
Known GenesSLC22A23
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3944425
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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