A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406305



Internal ID21063858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152820252..153112124hg38UCSC Ensembl
chr5:152199812..152491684hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38291873
hg19291873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127045
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406305
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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