A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9763724



Internal ID18391284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:168768789..168768947hg38UCSC Ensembl
Outerchr4:168768782..168768963hg38UCSC Ensembl
Innerchr4:169689940..169690098hg19UCSC Ensembl
Outerchr4:169689933..169690114hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3564977
Supporting Variants
Samples
Known GenesPALLD
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9763724
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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