A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3563756



Internal ID22432492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:31974549..31974549hg38UCSC Ensembl
chr4:31976171..31976171hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14314062
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3563756
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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