A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412991



Internal ID21070544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:114691901..114706600hg38UCSC Ensembl
chr5:114027598..114042297hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3814700
hg1914700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212449
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412991
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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