A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527185



Internal ID22396570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100001189..100001484hg38UCSC Ensembl
chr10:101760946..101761241hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14352931, nssv14352932, nssv14352934, nssv14352933
SamplesHG00512, NA19239, HG00731, HG00513
Known GenesDNMBP
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527185
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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