A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17564932



Internal ID21889287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151166574..151166574hg38UCSC Ensembl
chr5:150546135..150546135hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg382283
hg192283
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6077527
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17564932
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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