A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13549409



Internal ID1363177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88793432..88794303hg38UCSC Ensembl
Innerchr9:88793457..88794279hg38UCSC Ensembl
Outerchr9:88793408..88794328hg38UCSC Ensembl
chr9:91408347..91409218hg19UCSC Ensembl
Innerchr9:91408372..91409194hg19UCSC Ensembl
Outerchr9:91408323..91409243hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38872
hg19872
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621011
Supporting Variants
SamplesHG01204
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13549409
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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