A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3221646



Internal ID22365958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:87127940..87146706hg38UCSC Ensembl
chr15:87671171..87689937hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3818767
hg1918767
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14372671, nssv14392014, nssv14379198, nssv14392309
SamplesNA19238, NA19240, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3221646
Frequency
Sample Size9
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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