A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14299171



Internal ID22273050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:8846304..8886188hg38UCSC Ensembl
chr21:9735137..9775021hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3839885
hg1939885
Variant TypeOTHER copy number variation
Copy Number48
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3200789
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14299171
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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