A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18103751



Internal ID20670791
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 StatusS
Merged Variantsnsv6357343
Supporting Variants
Samples
Known GenesFOXP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18103751
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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