A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13638529



Internal ID3640345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132884570..132886716hg38UCSC Ensembl
Innerchr9:132884570..132886716hg38UCSC Ensembl
Outerchr9:132884431..132886781hg38UCSC Ensembl
chr9:135759957..135762103hg19UCSC Ensembl
Innerchr9:135759957..135762103hg19UCSC Ensembl
Outerchr9:135759818..135762168hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg382147
hg192147
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621926
Supporting Variants
SamplesHG03838
Known GenesC9orf9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13638529
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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