A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744273



Internal ID18371833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130268593..130271825hg38UCSC Ensembl
Outerchr9:130268222..130272645hg38UCSC Ensembl
Innerchr9:133030872..133034104hg19UCSC Ensembl
Outerchr9:133030501..133034924hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg384424
hg194424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545526
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744273
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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