A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9761676



Internal ID18735922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:174443771..174444042hg38UCSC Ensembl
Outerchr3:174443708..174444065hg38UCSC Ensembl
Innerchr3:174161561..174161832hg19UCSC Ensembl
Outerchr3:174161498..174161855hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38358
hg19358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3562929
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9761676
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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