A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9763135



Internal ID18390695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:106136041..106141200hg38UCSC Ensembl
Outerchr4:106134844..106142469hg38UCSC Ensembl
Innerchr4:107057198..107062357hg19UCSC Ensembl
Outerchr4:107056001..107063626hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg387626
hg197626
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3564388
Supporting Variants
Samples
Known GenesTBCK
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9763135
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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