A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893568



Internal ID18837702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:57618490..58256638hg38UCSC Ensembl
Outerchr1:57618490..58256638hg38UCSC Ensembl
Innerchr1:58084162..58722310hg19UCSC Ensembl
Outerchr1:58084162..58722310hg19UCSC Ensembl
Innerchr1:57856750..58494898hg18UCSC Ensembl
Outerchr1:57856750..58494898hg18UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg38638149
hg19638149
hg18638149
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789659
Samples
Known GenesDAB1, DAB1-AS1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893568
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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