A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15201809



Internal ID21340609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:143631224..143631224hg38UCSC Ensembl
chr5:143010789..143010789hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3937362
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15201809
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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