A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611759



Internal ID6998663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:159005..191283hg38UCSC Ensembl
chr7:159005..191283hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3832279
hg1932279
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12657169, essv12657167, essv12657168
SamplesNA19731, HG01797, HG03672
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611759
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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