A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3935963



Internal ID11479223
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1026000
Supporting Variants
SamplesHuRef
Known GenesTJP2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3935963
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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