A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379063



Internal ID21036616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:27900201..27935500hg38UCSC Ensembl
chr5:27900308..27935607hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3835300
hg1935300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5709n223
Supporting Variantsnssv18215767
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379063
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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