A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405380



Internal ID21062933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146522464..146527922hg38UCSC Ensembl
chr5:145902027..145907485hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg385459
hg195459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126050
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405380
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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