A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210652



Internal ID22358485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55218300..55218361hg38UCSC Ensembl
chr19:55729668..55729729hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14287038, nssv14287037
SamplesNA19239, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210652
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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