A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13589591



Internal ID2901084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:103340021..103420009hg38UCSC Ensembl
Innerchr9:103340039..103419992hg38UCSC Ensembl
Outerchr9:103340004..103420027hg38UCSC Ensembl
chr9:106102303..106182291hg19UCSC Ensembl
Innerchr9:106102321..106182274hg19UCSC Ensembl
Outerchr9:106102286..106182309hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3879989
hg1979989
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621310
Supporting Variants
SamplesHG02571
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13589591
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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