A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5858673



Internal ID9182305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38566749..38574683hg38UCSC Ensembl
chr1:39032421..39040355hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg387935
hg197935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673731
Supporting Variants
SamplesHG01440
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5858673
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