A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5796955



Internal ID8833522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39283565..39299944hg38UCSC Ensembl
Outerchr8:39283528..39299994hg38UCSC Ensembl
Innerchr8:39141084..39157463hg19UCSC Ensembl
Outerchr8:39141047..39157513hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3816467
hg1916467
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664833
Supporting Variants
SamplesHG00273
Known GenesADAM32
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5796955
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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