A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3565297



Internal ID18419687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:343253..343404hg38UCSC Ensembl
Outerchr5:343223..343420hg38UCSC Ensembl
Innerchr5:343368..343519hg19UCSC Ensembl
Outerchr5:343338..343535hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9764044
Samples
Known GenesAHRR
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3565297
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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