A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614486



Internal ID7001379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108954936..109000743hg38UCSC Ensembl
chr7:108594993..108640800hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3845808
hg1945808
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1317e214
Supporting Variantsessv12922642, essv12922640, essv12922643, essv12922641, essv12922644, essv12922639
SamplesNA18526, NA18633, NA19086, NA18956, HG00613, HG00446
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614486
Frequency
Sample Size2504
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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