A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613726



Internal ID6653935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75699055..75796413hg38UCSC Ensembl
chr7:75328373..75425731hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3897359
hg1997359
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12848040
SamplesNA20519
Known GenesCCL26, HIP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613726
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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