A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13628370



Internal ID4284850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129365246..129374271hg38UCSC Ensembl
Innerchr9:129365291..129374226hg38UCSC Ensembl
Outerchr9:129365201..129374316hg38UCSC Ensembl
chr9:132127525..132136550hg19UCSC Ensembl
Innerchr9:132127570..132136505hg19UCSC Ensembl
Outerchr9:132127480..132136595hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg389026
hg199026
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621832
Supporting Variants
SamplesHG03849
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13628370
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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