A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612269



Internal ID6999170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12889606..12952303hg38UCSC Ensembl
chr7:12929231..12991928hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3862698
hg1962698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1266e214
Supporting Variantsessv12683971
SamplesNA20911
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612269
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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