A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13408157



Internal ID3583078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15692086..15712888hg38UCSC Ensembl
Innerchr9:15692586..15712388hg38UCSC Ensembl
Outerchr9:15691086..15713888hg38UCSC Ensembl
chr9:15692084..15712886hg19UCSC Ensembl
Innerchr9:15692584..15712386hg19UCSC Ensembl
Outerchr9:15691084..15713886hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3820803
hg1920803
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619790
Supporting Variants
SamplesHG03168
Known GenesCCDC171
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13408157
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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