A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13682791



Internal ID4803914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4251261..4269421hg38UCSC Ensembl
Innerchr10:4251761..4268921hg38UCSC Ensembl
Outerchr10:4250261..4270421hg38UCSC Ensembl
chr10:4293453..4311613hg19UCSC Ensembl
Innerchr10:4293953..4311113hg19UCSC Ensembl
Outerchr10:4292453..4312613hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3818161
hg1918161
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622190
Supporting Variants
SamplesNA11992
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13682791
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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