A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382013



Internal ID21039566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:115373122..116074953hg38UCSC Ensembl
chr4:116294278..116996109hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38701832
hg19701832
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18107074
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382013
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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