A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525655



Internal ID22395033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:79352143..79352486hg38UCSC Ensembl
chr5:78647966..78648309hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7400n152
Supporting Variantsnssv14321971, nssv14321970, nssv14321969, nssv14321972
SamplesNA19238, NA19239, HG00731, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525655
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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