A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9764218



Internal ID18738464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:7221833..7222081hg38UCSC Ensembl
Outerchr5:7221813..7222144hg38UCSC Ensembl
Innerchr5:7221946..7222194hg19UCSC Ensembl
Outerchr5:7221926..7222257hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3565471
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9764218
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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