A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757535



Internal ID18731781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:24076525..24076769hg38UCSC Ensembl
Outerchr1:24076467..24076868hg38UCSC Ensembl
Innerchr1:24403015..24403259hg19UCSC Ensembl
Outerchr1:24402957..24403358hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558788
Supporting Variants
Samples
Known GenesMYOM3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757535
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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