A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374008



Internal ID21031561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58076695..58083485hg38UCSC Ensembl
chr3:58062422..58069212hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg386791
hg196791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102926
Samples
Known GenesFLNB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374008
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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