A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525440



Internal ID22394818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38326852..38326919hg38UCSC Ensembl
chr3:38368343..38368410hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14306004, nssv14306002, nssv14306003
SamplesNA19238, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525440
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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