A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891092



Internal ID18838802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:31337755..31437668hg38UCSC Ensembl
Outerchr7:31337755..31437668hg38UCSC Ensembl
Innerchr7:31377369..31477282hg19UCSC Ensembl
Outerchr7:31377369..31477282hg19UCSC Ensembl
Innerchr7:31343894..31443807hg18UCSC Ensembl
Outerchr7:31343894..31443807hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3899914
hg1999914
hg1899914
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789489
Samples
Known GenesNEUROD6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891092
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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