A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527709



Internal ID22397096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:70539389..70540255hg38UCSC Ensembl
chr8:71451624..71452490hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg38867
hg19867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14343061, nssv14343060
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527709
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