A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14358586



Internal ID22268750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76961781..76966776hg38UCSC Ensembl
chr11:76672825..76677820hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg384996
hg194996
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3528281
Supporting Variants
SamplesNA19238
Known GenesACER3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14358586
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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