A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3218014



Internal ID22363503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125319339..125319478hg38UCSC Ensembl
chr9:128081618..128081757hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14347719
SamplesHG00512
Known GenesGAPVD1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3218014
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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