A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199848



Internal ID22349382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:33848061..33851017hg38UCSC Ensembl
chr4:33849683..33852639hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg382957
hg192957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14314138, nssv14314139
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199848
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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