A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3190393



Internal ID22341266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61496610..61503884hg38UCSC Ensembl
chr1:61962282..61969556hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg387275
hg197275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14366125
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3190393
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer