A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3559030



Internal ID22427835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130969569..130969569hg38UCSC Ensembl
chr10:132767832..132767832hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14355018
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3559030
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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