A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1026000



Internal ID11842439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69123206..69128440hg38UCSC Ensembl
chr9:71738122..71743356hg19UCSC Ensembl
chr9:70927942..70933176hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg385235
hg195235
hg185235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3935963
SamplesHuRef
Known GenesTJP2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1026000
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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