A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3565071



Internal ID22433793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155590280..155590280hg38UCSC Ensembl
chr7:155382974..155382974hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14338755
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3565071
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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