A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13706123



Internal ID4097559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16412103..16419693hg38UCSC Ensembl
Innerchr10:16412153..16419643hg38UCSC Ensembl
Outerchr10:16412053..16419743hg38UCSC Ensembl
chr10:16454102..16461692hg19UCSC Ensembl
Innerchr10:16454152..16461642hg19UCSC Ensembl
Outerchr10:16454052..16461742hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg387591
hg197591
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622470
Supporting Variants
SamplesHG03720
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13706123
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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