A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6237941



Internal ID9105741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:191947036..191949292hg38UCSC Ensembl
Outerchr1:191946465..191949762hg38UCSC Ensembl
Innerchr1:191916166..191918422hg19UCSC Ensembl
Outerchr1:191915595..191918892hg19UCSC Ensembl
Cytoband1q31.2
Allele length
AssemblyAllele length
hg383298
hg193298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676880
Supporting Variants
SamplesHG01098
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6237941
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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