A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616810



Internal ID6657006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:32440011..32443792hg38UCSC Ensembl
chr8:32297527..32301308hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg383782
hg193782
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13156572
SamplesHG03788
Known GenesNRG1, NRG1-IT3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616810
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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