A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3208076



Internal ID22356372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155801625..155802005hg38UCSC Ensembl
chr1:155771416..155771796hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38381
hg19381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14289072, nssv14289071
SamplesNA19239, HG00732
Known GenesGON4L
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3208076
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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