A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526582



Internal ID22395963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:103694209..103694402hg38UCSC Ensembl
chr4:104615366..104615559hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14316202
SamplesNA19239
Known GenesTACR3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526582
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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