A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527704



Internal ID22397091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129361264..129362092hg38UCSC Ensembl
chr9:132123543..132124371hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38829
hg19829
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14348484, nssv14348483, nssv14348482
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527704
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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