A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3207996



Internal ID22356306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:152111644..152111747hg38UCSC Ensembl
chr4:153032796..153032899hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6892n152
Supporting Variantsnssv14318958, nssv14318959
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3207996
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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