A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619945



Internal ID7006818
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13416437, essv13416438
SamplesHG01896, NA19144
Known GenesFOCAD
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619945
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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