A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13628251



Internal ID5180276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129302787..129305145hg38UCSC Ensembl
Innerchr9:129302788..129305145hg38UCSC Ensembl
Outerchr9:129302787..129305146hg38UCSC Ensembl
chr9:132065066..132067424hg19UCSC Ensembl
Innerchr9:132065067..132067424hg19UCSC Ensembl
Outerchr9:132065066..132067425hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg382359
hg192359
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621829
Supporting Variants
SamplesNA18605
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13628251
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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