A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347663



Internal ID21005216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:112480701..112482900hg38UCSC Ensembl
chr2:113238278..113240477hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206487
Samples
Known GenesTTL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347663
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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