A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9749093



Internal ID18723339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:39360082..39361096hg38UCSC Ensembl
Outerchr13:39360015..39361358hg38UCSC Ensembl
Innerchr13:39934219..39935233hg19UCSC Ensembl
Outerchr13:39934152..39935495hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381344
hg191344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3550346
Supporting Variants
Samples
Known GenesLHFP
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9749093
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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