A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380958



Internal ID21038511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:39105587..39106050hg38UCSC Ensembl
chr5:39105689..39106152hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38464
hg19464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18130764
Samples
Known GenesFYB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380958
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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