A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614487



Internal ID7001380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108955752..109004438hg38UCSC Ensembl
chr7:108595809..108644495hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3848687
hg1948687
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1317e214
Supporting Variantsessv12922648, essv12922645, essv12922646, essv12922647
SamplesNA18526, NA18633, NA18956, HG00446
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614487
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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