A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14358803



Internal ID22271627
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3227541
Supporting Variants
SamplesNA19239
Known GenesIPO7
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14358803
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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