A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5449538



Internal ID8808391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:75875652..75879630hg38UCSC Ensembl
Outerchr9:75875495..75879783hg38UCSC Ensembl
Innerchr9:78490568..78494546hg19UCSC Ensembl
Outerchr9:78490411..78494699hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg384289
hg194289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662282
Supporting Variants
SamplesHG00252
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5449538
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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