A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357343



Internal ID21014896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71390546..71407870hg38UCSC Ensembl
chr3:71439697..71457021hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3817325
hg1917325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103751
Samples
Known GenesFOXP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357343
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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