A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9746402



Internal ID18373962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:226978538..226978741hg38UCSC Ensembl
Outerchr1:226978490..226978788hg38UCSC Ensembl
Innerchr1:227166239..227166442hg19UCSC Ensembl
Outerchr1:227166191..227166489hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3547655
Supporting Variants
Samples
Known GenesADCK3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9746402
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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