A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13635932



Internal ID3002055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132666804..132668646hg38UCSC Ensembl
Innerchr9:132666804..132668646hg38UCSC Ensembl
Outerchr9:132666552..132668986hg38UCSC Ensembl
chr9:135542191..135544033hg19UCSC Ensembl
Innerchr9:135542191..135544033hg19UCSC Ensembl
Outerchr9:135541939..135544373hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg381843
hg191843
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621918
Supporting Variants
SamplesHG02648
Known GenesDDX31
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13635932
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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