A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380778



Internal ID21038331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14879944..14886031hg38UCSC Ensembl
chr5:14880053..14886140hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg386088
hg196088
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125964
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380778
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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