A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7537396



Internal ID10468992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:69123206..69128440hg38UCSC Ensembl
Outerchr9:71738122..71743356hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg385235
hg195235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3267829
Supporting Variants
SamplesHuRef
Known GenesTJP2
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7537396
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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