A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478440



Internal ID21135993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:114346301..114347000hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007563
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478440
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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