A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6043438



Internal ID9740627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:138450492..138452475hg38UCSC Ensembl
Outerchr7:138450335..138452628hg38UCSC Ensembl
Innerchr7:138135237..138137220hg19UCSC Ensembl
Outerchr7:138135080..138137373hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg382294
hg192294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674762
Supporting Variants
SamplesNA19676
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6043438
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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