A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340032



Internal ID20997585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:168214123..168288032hg38UCSC Ensembl
chr2:169070633..169144542hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3873910
hg1973910
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207375
Samples
Known GenesSTK39
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340032
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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