A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13682792



Internal ID2320701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4251262..4270347hg38UCSC Ensembl
chr10:4293454..4312539hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3819086
hg1919086
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622191
Supporting Variants
SamplesHG02067
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13682792
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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