A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6447576



Internal ID9839049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:153182736..153207930hg38UCSC Ensembl
Outerchr6:153182699..153207980hg38UCSC Ensembl
Innerchr6:153503871..153529065hg19UCSC Ensembl
Outerchr6:153503834..153529115hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3825282
hg1925282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2660456
Supporting Variants
SamplesNA20503
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6447576
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