A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9761452



Internal ID18735698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149246045..149251269hg38UCSC Ensembl
Outerchr3:149245107..149252213hg38UCSC Ensembl
Innerchr3:148963832..148969056hg19UCSC Ensembl
Outerchr3:148962894..148970000hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg387107
hg197107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3562705
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9761452
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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