A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3195742



Internal ID22345874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:212202072..212202437hg38UCSC Ensembl
chr1:212375414..212375779hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg38366
hg19366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14306034
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3195742
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