A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616802



Internal ID6656998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:31672956..31686929hg38UCSC Ensembl
chr8:31530472..31544445hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3813974
hg1913974
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13156524
SamplesHG00705
Known GenesNRG1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616802
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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