A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525178



Internal ID22394554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149079463..149079517hg38UCSC Ensembl
chr3:148797250..148797304hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14308225, nssv14308226, nssv14308228, nssv14308227
SamplesNA19239, HG00731, NA19240, HG00733
Known GenesHLTF
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525178
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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