A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6587885



Internal ID9515563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:115858922..115863802hg38UCSC Ensembl
Outerchr7:115858885..115863852hg38UCSC Ensembl
Innerchr7:115498976..115503856hg19UCSC Ensembl
Outerchr7:115498939..115503906hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg384968
hg194968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663889
Supporting Variants
SamplesNA19002
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6587885
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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