A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14349536



Internal ID22206728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137439701..137452800hg38UCSC Ensembl
chr9:140334153..140347252hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3813100
hg1913100
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3212637
Supporting Variants
SamplesHG00732
Known GenesENTPD8, MIR7114, NSMF
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14349536
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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