A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9754173



Internal ID18381733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:55245763..55245886hg38UCSC Ensembl
Outerchr18:55245760..55245894hg38UCSC Ensembl
Innerchr18:52912994..52913117hg19UCSC Ensembl
Outerchr18:52912991..52913125hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3555426
Supporting Variants
Samples
Known GenesTCF4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9754173
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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