A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3929800



Internal ID21349870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112138242..112138242hg38UCSC Ensembl
chr9:114900522..114900522hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15205844
SamplesHG002
Known GenesMIR3134, SUSD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3929800
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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