A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6226289



Internal ID9203692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:1503276..1504209hg38UCSC Ensembl
chr8:1451442..1452375hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38934
hg19934
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667804
Supporting Variants
SamplesNA19431
Known GenesDLGAP2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6226289
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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