A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9764777



Internal ID18739023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:65732462..65734307hg38UCSC Ensembl
Outerchr5:65732186..65734700hg38UCSC Ensembl
Innerchr5:65028289..65030134hg19UCSC Ensembl
Outerchr5:65028013..65030527hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg382515
hg192515
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3566030
Supporting Variants
Samples
Known GenesNLN
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9764777
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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