A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9762879



Internal ID18390439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:79967165..79972916hg38UCSC Ensembl
Outerchr4:79966825..79973047hg38UCSC Ensembl
Innerchr4:80888319..80894070hg19UCSC Ensembl
Outerchr4:80887979..80894201hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg386223
hg196223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3564132
Supporting Variants
Samples
Known GenesANTXR2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9762879
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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