A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206536



Internal ID22355058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:119798319..119798391hg38UCSC Ensembl
chr6:120119465..120119537hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8074n152
Supporting Variantsnssv14331996, nssv14331994, nssv14331995
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206536
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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