A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6003294



Internal ID9078245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:73073483..73263988hg38UCSC Ensembl
Outerchr1:73073326..73264141hg38UCSC Ensembl
Innerchr1:73539166..73729671hg19UCSC Ensembl
Outerchr1:73539009..73729824hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38190816
hg19190816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674879
Supporting Variants
SamplesHG01052
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6003294
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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