A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527355



Internal ID22396740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:12456858..12457387hg38UCSC Ensembl
chr12:12609792..12610321hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38530
hg19530
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14360285, nssv14360286
SamplesNA19239, HG00732
Known GenesLOH12CR1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527355
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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