A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665648



Internal ID9931753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:135678137..135679900hg38UCSC Ensembl
chr7:135362885..135364648hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg381764
hg191764
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6139053, essv6036053, essv6419882, essv6028877
SamplesNA19466, NA19914, NA19440, NA19835
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665648
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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