A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339645



Internal ID20997198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:109139402..109140596hg38UCSC Ensembl
chr2:109755858..109757052hg19UCSC Ensembl
Cytoband2q12.3
Allele length
AssemblyAllele length
hg381195
hg191195
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204000
Samples
Known GenesSH3RF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339645
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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