A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527543



Internal ID22396930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97787744..97787812hg38UCSC Ensembl
chr14:98254081..98254149hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2735n152
Supporting Variantsnssv14387764, nssv14391128, nssv14379949, nssv14379421
SamplesHG00512, NA19239, NA19240, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527543
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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