A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13093741



Internal ID3095557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8901663..9165103hg38UCSC Ensembl
chr8:8759173..9022613hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38263441
hg19263441
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3616157
Supporting Variants
SamplesNA20761
Known GenesERI1, MIR4660, PPP1R3B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13093741
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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