A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9761857



Internal ID18736103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:192641138..192641404hg38UCSC Ensembl
Outerchr3:192641072..192641445hg38UCSC Ensembl
Innerchr3:192358927..192359193hg19UCSC Ensembl
Outerchr3:192358861..192359234hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38374
hg19374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3563110
Supporting Variants
Samples
Known GenesFGF12
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9761857
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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