A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376831



Internal ID21034384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:39715801..39725800hg38UCSC Ensembl
chr5:39715903..39725902hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3810000
hg1910000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213462
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376831
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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