A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13628414



Internal ID2721801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129642396..129643137hg38UCSC Ensembl
Innerchr9:129642396..129643137hg38UCSC Ensembl
Outerchr9:129642087..129643392hg38UCSC Ensembl
chr9:132404675..132405416hg19UCSC Ensembl
Innerchr9:132404675..132405416hg19UCSC Ensembl
Outerchr9:132404366..132405671hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38742
hg19742
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621838
Supporting Variants
SamplesHG02397
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13628414
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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