A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226719



Internal ID22369431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129499622..129499843hg38UCSC Ensembl
chr9:132261901..132262122hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14348494
SamplesNA19239
Known GenesLINC00963
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226719
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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