A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17414518



Internal ID22472388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6321538..6321538hg38UCSC Ensembl
chr5:6321651..6321651hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5966817
Supporting Variants
Samples
Known GenesFLJ33360
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17414518
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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