A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14359716



Internal ID22270269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61484531..61484620hg38UCSC Ensembl
chr11:61252003..61252092hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3212332
Supporting Variants
SamplesNA19239
Known GenesPPP1R32
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14359716
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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