A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14347699



Internal ID22255136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125076611..125076994hg38UCSC Ensembl
chr9:127838890..127839273hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529681
Supporting Variants
SamplesNA19238
Known GenesSCAI
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14347699
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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