A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7104914



Internal ID10383196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:99909938..99910787hg38UCSC Ensembl
Outerchr3:99628782..99629631hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38850
hg19850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2835347
Supporting Variants
SamplesHuRef
Known GenesCMSS1, FILIP1L, MIR548G
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7104914
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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