A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3559485



Internal ID22428286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7331215..7331215hg38UCSC Ensembl
chr11:7352446..7352446hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14358100, nssv14358101
SamplesHG00731, HG00732
Known GenesSYT9
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3559485
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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