A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339247



Internal ID20996800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3477335..3496795hg38UCSC Ensembl
chr2:3481106..3500566hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3819461
hg1919461
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206872
Samples
Known GenesTRAPPC12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339247
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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