A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528924



Internal ID22398317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:64332681..64333034hg38UCSC Ensembl
chr14:64799399..64799752hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg38354
hg19354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14370317, nssv14370315, nssv14370316
SamplesHG00731, HG00733, HG00514
Known GenesESR2, MIR548AZ
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528924
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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