A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619461



Internal ID7006335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:7288357..7371938hg38UCSC Ensembl
Innerchr9:7288370..7371925hg38UCSC Ensembl
Outerchr9:7288344..7371951hg38UCSC Ensembl
chr9:7288357..7371938hg19UCSC Ensembl
Innerchr9:7288370..7371925hg19UCSC Ensembl
Outerchr9:7288344..7371951hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3883582
hg1983582
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1436e214
Supporting Variantsessv13391189
SamplesNA18608
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619461
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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