A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14358532



Internal ID22268738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:41482578..41488990hg38UCSC Ensembl
chr11:41504128..41510540hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg386413
hg196413
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3222796
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14358532
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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