A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5907117



Internal ID9479368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:63241881..63243451hg38UCSC Ensembl
chr8:64154439..64156009hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg381571
hg191571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672463
Supporting Variants
SamplesNA18950
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5907117
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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