A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6229162



Internal ID9416680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25573853..25581550hg38UCSC Ensembl
chr1:25900344..25908041hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg387698
hg197698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2656499
Supporting Variants
SamplesNA18618
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6229162
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