A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5655230



Internal ID9538036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:35708644..35714139hg38UCSC Ensembl
Outerchr10:35708487..35714292hg38UCSC Ensembl
Innerchr10:35997572..36003067hg19UCSC Ensembl
Outerchr10:35997415..36003220hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg385806
hg195806
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671892
Supporting Variants
SamplesNA19067
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5655230
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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