A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13814082



Internal ID1575031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:53286669..53450075hg38UCSC Ensembl
chr10:55046429..55209835hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38163407
hg19163407
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623284
Supporting Variants
SamplesHG01459
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13814082
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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