A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614276



Internal ID7001171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99306477..99318899hg38UCSC Ensembl
chr7:98904100..98916522hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3812423
hg1912423
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12906294, essv12906295, essv12906293, essv12906296, essv12906292
SamplesNA19076, NA18993, NA18960, NA18531, NA19003
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614276
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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