A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3563748



Internal ID22432484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37901687..37901687hg38UCSC Ensembl
chr4:37903308..37903308hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14314894, nssv14314893
SamplesNA19238, NA19240
Known GenesTBC1D1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3563748
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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