A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13411501



Internal ID6561130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:16988089..17064870hg38UCSC Ensembl
Innerchr9:16988089..17064870hg38UCSC Ensembl
Outerchr9:16987994..17064942hg38UCSC Ensembl
chr9:16988087..17064868hg19UCSC Ensembl
Innerchr9:16988087..17064868hg19UCSC Ensembl
Outerchr9:16987992..17064940hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3876782
hg1976782
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619828
Supporting Variants
SamplesNA20756
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13411501
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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