A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15202219



Internal ID21341018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:108690880..108690880hg38UCSC Ensembl
chr5:108026581..108026581hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3936251
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15202219
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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