A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526137



Internal ID22395517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:156660547..156660684hg38UCSC Ensembl
chr4:157581699..157581836hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14316985
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526137
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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