A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3192323



Internal ID22342927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:5667636..5667832hg38UCSC Ensembl
chr1:5727696..5727892hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv81n152
Supporting Variantsnssv14303089
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3192323
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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