A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9763198



Internal ID18390758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:112548834..112549122hg38UCSC Ensembl
Outerchr4:112548769..112549173hg38UCSC Ensembl
Innerchr4:113469990..113470278hg19UCSC Ensembl
Outerchr4:113469925..113470329hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3564451
Supporting Variants
Samples
Known GenesC4orf21
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9763198
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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