A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6086207



Internal ID9057351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72686529..72687636hg38UCSC Ensembl
chr3:72735680..72736787hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381108
hg191108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663075
Supporting Variants
SamplesHG00704
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6086207
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