A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6472879



Internal ID8873523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:110508312..110512254hg38UCSC Ensembl
Outerchr7:110508155..110512407hg38UCSC Ensembl
Innerchr7:110148369..110152311hg19UCSC Ensembl
Outerchr7:110148212..110152464hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg384253
hg194253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658662
Supporting Variants
SamplesHG00326
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6472879
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