A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13451452



Internal ID4996754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33015432..33023864hg38UCSC Ensembl
Innerchr9:33015432..33023864hg38UCSC Ensembl
Outerchr9:33015348..33023897hg38UCSC Ensembl
chr9:33015430..33023862hg19UCSC Ensembl
Innerchr9:33015430..33023862hg19UCSC Ensembl
Outerchr9:33015346..33023895hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg388433
hg198433
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620315
Supporting Variants
SamplesNA18501
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13451452
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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