A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675550



Internal ID9941655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:64022454..64278994hg38UCSC Ensembl
chr7:63482832..63739372hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38256541
hg19256541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1212e199
Supporting Variantsessv6411359, essv5623430, essv5786703
SamplesNA20507, NA18532, NA19012
Known GenesLINC01005, ZNF679, ZNF727, ZNF735
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675550
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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