A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7536951



Internal ID10815233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:81806343..81808335hg38UCSC Ensembl
Outerchr9:84421258..84423250hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg381993
hg191993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3267384
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7536951
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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