A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081578



Internal ID21990811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18212717..18212717hg38UCSC Ensembl
chrUn_gl000212:41469..41469hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381267
hg191267
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609228
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081578
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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