A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9762901



Internal ID18737147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:82993804..82998320hg38UCSC Ensembl
Outerchr4:82992804..82998360hg38UCSC Ensembl
Innerchr4:83914957..83919473hg19UCSC Ensembl
Outerchr4:83913957..83919513hg19UCSC Ensembl
Cytoband4q21.22
Allele length
AssemblyAllele length
hg385557
hg195557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3564154
Supporting Variants
Samples
Known GenesLIN54
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9762901
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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