A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386269



Internal ID21043822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7977646..7991438hg38UCSC Ensembl
chr5:7977759..7991551hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3813793
hg1913793
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214192
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386269
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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