A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415203



Internal ID21072756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:112967449..112988359hg38UCSC Ensembl
chr5:112303146..112324056hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg3820911
hg1920911
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212432
Samples
Known GenesDCP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415203
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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