A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377882



Internal ID21035435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17024284..17094386hg38UCSC Ensembl
chr5:17024393..17094495hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3870103
hg1970103
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216392
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377882
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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