A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526397



Internal ID22395778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:41226717..41243850hg38UCSC Ensembl
chr5:41226819..41243952hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3817134
hg1917134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7302n152
Supporting Variantsnssv14320006
SamplesHG00512
Known GenesC6
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526397
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