A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6407632



Internal ID9680747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84699704..84700508hg38UCSC Ensembl
chr15:85242935..85243739hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38805
hg19805
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2672412
Supporting Variants
SamplesNA19431
Known GenesSEC11A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6407632
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