A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891780



Internal ID19186176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:31443082..31525030hg38UCSC Ensembl
Outerchr10:31443082..31525030hg38UCSC Ensembl
Innerchr10:31732011..31813958hg19UCSC Ensembl
Outerchr10:31732011..31813958hg19UCSC Ensembl
Innerchr10:31772017..31853964hg18UCSC Ensembl
Outerchr10:31772017..31853964hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3881949
hg1981948
hg1881948
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790307
Samples
Known GenesZEB1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891780
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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