A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14348484



Internal ID22317947
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527704
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14348484
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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