A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744308



Internal ID18718554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133019415..133021186hg38UCSC Ensembl
Outerchr9:133019398..133021249hg38UCSC Ensembl
Innerchr9:135894802..135896573hg19UCSC Ensembl
Outerchr9:135894785..135896636hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg381852
hg191852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545561
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744308
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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