A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620003



Internal ID7006876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:22967618..23019252hg38UCSC Ensembl
Innerchr9:22967631..23019240hg38UCSC Ensembl
Outerchr9:22967606..23019265hg38UCSC Ensembl
chr9:22967617..23019251hg19UCSC Ensembl
Innerchr9:22967630..23019239hg19UCSC Ensembl
Outerchr9:22967605..23019264hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3851635
hg1951635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13428352
SamplesNA18878
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620003
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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