A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9760102



Internal ID18387662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2454072..2454520hg38UCSC Ensembl
Outerchr3:2453974..2454732hg38UCSC Ensembl
Innerchr3:2495756..2496204hg19UCSC Ensembl
Outerchr3:2495658..2496416hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38759
hg19759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3561355
Supporting Variants
Samples
Known GenesCNTN4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9760102
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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