A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17572998



Internal ID21765041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151278303..151278303hg38UCSC Ensembl
chr5:150657864..150657864hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6076790
Supporting Variants
Samples
Known GenesSLC36A3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17572998
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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