A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13436623



Internal ID4680501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28373198..28412495hg38UCSC Ensembl
Innerchr9:28373208..28412485hg38UCSC Ensembl
Outerchr9:28373188..28412505hg38UCSC Ensembl
chr9:28373196..28412493hg19UCSC Ensembl
Innerchr9:28373206..28412483hg19UCSC Ensembl
Outerchr9:28373186..28412503hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3839298
hg1939298
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620157
Supporting Variants
SamplesHG04206
Known GenesLINGO2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13436623
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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