A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369731



Internal ID21027284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71320547..71325014hg38UCSC Ensembl
chr3:71369698..71374165hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg384468
hg194468
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103748
Samples
Known GenesFOXP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369731
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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