A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613886



Internal ID7000781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81370337..81412456hg38UCSC Ensembl
chr7:80999653..81041772hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3842120
hg1942120
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12864815
SamplesHG04118
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613886
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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