A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5777636



Internal ID8755039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:9156428..9230320hg38UCSC Ensembl
chr4:9158154..9232046hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3873893
hg1973893
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668726
Supporting Variants
SamplesNA19704
Known GenesUSP17L10, USP17L11, USP17L12, USP17L13, USP17L18, USP17L20, USP17L21
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5777636
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