A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635964



Internal ID7022761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:27067125..27074462hg38UCSC Ensembl
chr15:27312272..27319609hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg387338
hg197338
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15195268, essv15195266, essv15195267
SamplesHG01444, HG02681, HG02348
Known GenesGABRG3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635964
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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