A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3564932



Internal ID22433656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124455068..124455068hg38UCSC Ensembl
chr8:125467309..125467309hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14344923, nssv14344922
SamplesHG00512, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3564932
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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