A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595666



Internal ID6982984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27251911..27278375hg38UCSC Ensembl
chr3:27293402..27319866hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3826465
hg1926465
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10961151
SamplesHG03369
Known GenesNEK10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595666
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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