A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394642



Internal ID21052195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:4771954..4787031hg38UCSC Ensembl
chr5:4772067..4787144hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg3815078
hg1915078
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213996
Samples
Known GenesLOC101929153
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394642
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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