A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387881



Internal ID21045434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:4857151..4892304hg38UCSC Ensembl
chr5:4857264..4892417hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg3835154
hg1935154
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213999
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387881
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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