A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3629111



Internal ID7015933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:33365136..33425922hg38UCSC Ensembl
chr12:33518071..33578857hg19UCSC Ensembl
Cytoband12p11.1
Allele length
AssemblyAllele length
hg3860787
hg1960787
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv267e214
Supporting Variantsessv14441699, essv14441698
SamplesNA07357, HG02721
Known GenesSYT10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3629111
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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