A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17411293



Internal ID22469163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14927629..14927693hg38UCSC Ensembl
chr3:14969136..14969200hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5900035
Supporting Variants
Samples
Known GenesFGD5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17411293
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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