A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9762213



Internal ID18736459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15656679..15657009hg38UCSC Ensembl
Outerchr4:15656669..15657012hg38UCSC Ensembl
Innerchr4:15658302..15658632hg19UCSC Ensembl
Outerchr4:15658292..15658635hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3563466
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9762213
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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