A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17429608



Internal ID22487478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:169051415..169051415hg38UCSC Ensembl
chr5:168478420..168478420hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5964241
Supporting Variants
Samples
Known GenesSLIT3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17429608
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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