A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347851



Internal ID21005404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:109200798..109215015hg38UCSC Ensembl
chr2:109817254..109831471hg19UCSC Ensembl
Cytoband2q12.3
Allele length
AssemblyAllele length
hg3814218
hg1914218
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204003
Samples
Known GenesSH3RF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347851
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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