A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414322



Internal ID21071875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:78749691..78756487hg38UCSC Ensembl
chr5:78045514..78052310hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg386797
hg196797
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133381
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414322
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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