A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3209547



Internal ID22357604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:103418242..103426708hg38UCSC Ensembl
chr4:104339399..104347865hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg388467
hg198467
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14316183, nssv14316184
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3209547
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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