A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9764319



Internal ID18738565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:16124782..16125374hg38UCSC Ensembl
Outerchr5:16124639..16125392hg38UCSC Ensembl
Innerchr5:16124891..16125483hg19UCSC Ensembl
Outerchr5:16124748..16125501hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38754
hg19754
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3565572
Supporting Variants
Samples
Known GenesMARCH11
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9764319
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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