A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14347752



Internal ID22204369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126484534..126485603hg38UCSC Ensembl
chr9:129246813..129247882hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381070
hg191070
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529079
Supporting Variants
SamplesHG00732
Known GenesMVB12B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14347752
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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