A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14357337



Internal ID22275907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3961134..3961625hg38UCSC Ensembl
chr11:3982364..3982855hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38492
hg19492
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527795
Supporting Variants
SamplesNA19239
Known GenesSTIM1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14357337
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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