A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7107803



Internal ID10039399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:2269905..2270253hg38UCSC Ensembl
Outerchr3:2311589..2311937hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2838236
Supporting Variants
SamplesHuRef
Known GenesCNTN4
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7107803
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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