A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9749750



Internal ID18723996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:103279313..103279603hg38UCSC Ensembl
Outerchr13:103279266..103279627hg38UCSC Ensembl
Innerchr13:103931663..103931953hg19UCSC Ensembl
Outerchr13:103931616..103931977hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38362
hg19362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3551003
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9749750
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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