A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9749388



Internal ID18723634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68913447..68914173hg38UCSC Ensembl
Outerchr13:68913439..68914315hg38UCSC Ensembl
Innerchr13:69487579..69488305hg19UCSC Ensembl
Outerchr13:69487571..69488447hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38877
hg19877
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3550641
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9749388
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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