A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613758



Internal ID7000653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76131690..76161789hg38UCSC Ensembl
chr7:75761008..75791107hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3830100
hg1930100
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1304e214
Supporting Variantsessv12848876, essv12848877
SamplesNA07056, HG01111
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613758
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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