A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199981



Internal ID22349494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:41531634..41531842hg38UCSC Ensembl
chr1:41997305..41997513hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38209
hg19209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv193n152
Supporting Variantsnssv14363037, nssv14363039, nssv14363038
SamplesNA19238, NA19239, NA19240
Known GenesHIVEP3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199981
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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