A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400377



Internal ID21057930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152845964..152846433hg38UCSC Ensembl
chr5:152225524..152225993hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127048
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400377
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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