A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17408596



Internal ID22466466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:92943658..92954239hg38UCSC Ensembl
chr1:93409215..93419796hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg3810582
hg1910582
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5886140
Supporting Variants
Samples
Known GenesFAM69A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17408596
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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