A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225074



Internal ID22368314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99661965..99688450hg38UCSC Ensembl
chr10:101421722..101448207hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3826486
hg1926486
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14352925
SamplesNA19238
Known GenesENTPD7
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225074
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