A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9763151



Internal ID18737397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:107053173..107053328hg38UCSC Ensembl
Outerchr4:107053154..107053349hg38UCSC Ensembl
Innerchr4:107974330..107974485hg19UCSC Ensembl
Outerchr4:107974311..107974506hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3564404
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9763151
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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