A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3564186



Internal ID22432918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77097685..77097685hg38UCSC Ensembl
chr5:76393510..76393510hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14321832
SamplesHG00733
Known GenesZBED3-AS1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3564186
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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