A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671152



Internal ID9590571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:160822491..160822701hg38UCSC Ensembl
Outerchr1:160822454..160822751hg38UCSC Ensembl
Innerchr1:160792281..160792491hg19UCSC Ensembl
Outerchr1:160792244..160792541hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6576042
SamplesHG01101
Known GenesLY9
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671152
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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