A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9847n152



Internal ID22825550
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3212637, nsv3230262
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesENTPD8, MIR7114, NSMF
MethodMerging
Sequencing
AnalysisMultiple analysis algorthms
PhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformIllumina HiSeq
See merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv9847n152
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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