A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13416437



Internal ID2093863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:20958185..20972463hg38UCSC Ensembl
Innerchr9:20958227..20972421hg38UCSC Ensembl
Outerchr9:20958143..20972505hg38UCSC Ensembl
chr9:20958184..20972462hg19UCSC Ensembl
Innerchr9:20958226..20972420hg19UCSC Ensembl
Outerchr9:20958142..20972504hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3814279
hg1914279
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619945
Supporting Variants
SamplesHG01896
Known GenesFOCAD
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13416437
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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