A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3567091



Internal ID18768167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:178921554..178925531hg38UCSC Ensembl
Outerchr5:178921000..178926310hg38UCSC Ensembl
Innerchr5:178348555..178352532hg19UCSC Ensembl
Outerchr5:178348001..178353311hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg385311
hg195311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9765838
Samples
Known GenesZFP2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3567091
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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