A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206432



Internal ID22354973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:163574156..163574235hg38UCSC Ensembl
chr5:163001162..163001241hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7593n152
Supporting Variantsnssv14325258, nssv14325259, nssv14325257
SamplesHG00512, HG00731, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206432
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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