A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3196060



Internal ID22346140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32907032..32916350hg38UCSC Ensembl
chr1:33372633..33381951hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg389319
hg199319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14360925, nssv14360924, nssv14360926
SamplesHG00512, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3196060
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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