A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9749619



Internal ID18723865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:90495862..90495961hg38UCSC Ensembl
Outerchr13:90495858..90495979hg38UCSC Ensembl
Innerchr13:91148116..91148215hg19UCSC Ensembl
Outerchr13:91148112..91148233hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3550872
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9749619
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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