A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3541067



Internal ID18395457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:155874524..155875220hg38UCSC Ensembl
Outerchr1:155874376..155875302hg38UCSC Ensembl
Innerchr1:155844315..155845011hg19UCSC Ensembl
Outerchr1:155844167..155845093hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38927
hg19927
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9739814
Samples
Known GenesSYT11
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3541067
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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