A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7102581



Internal ID10380863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:149550689..149552364hg38UCSC Ensembl
Outerchr3:149268476..149270151hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg381676
hg191676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2833014
Supporting Variants
SamplesHuRef
Known GenesWWTR1
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7102581
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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