A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664653



Internal ID9930758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186631287..186631679hg38UCSC Ensembl
chr4:187552441..187552833hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38393
hg19393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6006241, essv6430185
SamplesNA19917, NA19213
Known GenesFAT1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664653
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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