A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14357174



Internal ID22182368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1656501..1669500hg38UCSC Ensembl
chr11:1677731..1690730hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3813000
hg1913000
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3213081
Supporting Variants
SamplesHG00514
Known GenesFAM99A, MOB2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14357174
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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