A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614637



Internal ID7001530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:112929644..112959300hg38UCSC Ensembl
chr7:112569699..112599355hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3829657
hg1929657
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12931121
SamplesNA19098
Known GenesC7orf60
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614637
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer