A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9758312



Internal ID18732558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:24852510..24857416hg38UCSC Ensembl
Outerchr1:24852010..24857536hg38UCSC Ensembl
Innerchr1:25179001..25183907hg19UCSC Ensembl
Outerchr1:25178501..25184027hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg385527
hg195527
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559565
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9758312
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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