A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3215339



Internal ID22361706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:33971120..33971647hg38UCSC Ensembl
chr14:34440326..34440853hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg38528
hg19528
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14370883, nssv14370880, nssv14370882, nssv14370881
SamplesHG00512, NA19239, HG00731, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3215339
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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