A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5527488



Internal ID9649187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92598033..92599086hg38UCSC Ensembl
chr7:92227347..92228400hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg381054
hg191054
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2665857
Supporting Variants
SamplesNA19381
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5527488
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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