A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612758



Internal ID6999658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:33091449..33149398hg38UCSC Ensembl
chr7:33131061..33189010hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3857950
hg1957950
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1278e214
Supporting Variantsessv12722386, essv12722385, essv12722387
SamplesHG00641, HG00155, HG00353
Known GenesBBS9, RP9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612758
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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