A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3227541



Internal ID22370004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9395796..9396355hg38UCSC Ensembl
chr11:9417343..9417902hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14358803
SamplesNA19239
Known GenesIPO7
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3227541
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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