A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619344



Internal ID7006222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4451776..4458112hg38UCSC Ensembl
Innerchr9:4451817..4458072hg38UCSC Ensembl
Outerchr9:4451736..4458153hg38UCSC Ensembl
chr9:4451776..4458112hg19UCSC Ensembl
Innerchr9:4451817..4458072hg19UCSC Ensembl
Outerchr9:4451736..4458153hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg386337
hg196337
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13383223, essv13383224
SamplesNA18858, HG03940
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619344
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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