A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658182



Internal ID9924287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96911907..96922016hg38UCSC Ensembl
chr5:96247611..96257720hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3810110
hg1910110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5506651, essv6597475
SamplesNA19068, NA18983
Known GenesERAP2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658182
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