A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9764624



Internal ID18392184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:44795002..44795376hg38UCSC Ensembl
Outerchr5:44794875..44795536hg38UCSC Ensembl
Innerchr5:44795104..44795478hg19UCSC Ensembl
Outerchr5:44794977..44795638hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38662
hg19662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3565877
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9764624
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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