A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339151



Internal ID20996704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3217862..3254943hg38UCSC Ensembl
chr2:3221633..3258714hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3837082
hg1937082
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208199
Samples
Known GenesTSSC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339151
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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