A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3561699



Internal ID18416089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:32297592..32298332hg38UCSC Ensembl
Outerchr3:32297446..32298360hg38UCSC Ensembl
Innerchr3:32339084..32339824hg19UCSC Ensembl
Outerchr3:32338938..32339852hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38915
hg19915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9760446
Samples
Known GenesCMTM8
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3561699
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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