A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3565324



Internal ID22434045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94049305..94049305hg38UCSC Ensembl
chr8:95061533..95061533hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14342783, nssv14342784
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3565324
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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