A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9765731



Internal ID18393291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:168967443..168967731hg38UCSC Ensembl
Outerchr5:168967406..168967757hg38UCSC Ensembl
Innerchr5:168394448..168394736hg19UCSC Ensembl
Outerchr5:168394411..168394762hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3566984
Supporting Variants
Samples
Known GenesSLIT3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9765731
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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