A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6206881



Internal ID9184284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:153517956..153519951hg38UCSC Ensembl
Outerchr5:153517799..153520104hg38UCSC Ensembl
Innerchr5:152897516..152899511hg19UCSC Ensembl
Outerchr5:152897359..152899664hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg382306
hg192306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2674452
Supporting Variants
SamplesHG00448
Known GenesGRIA1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6206881
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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