A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528440



Internal ID22397828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71265406..71267482hg38UCSC Ensembl
chr6:71975109..71977185hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg382077
hg192077
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7960n152
Supporting Variantsnssv14329270, nssv14329269
SamplesHG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528440
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