A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13870187



Internal ID5243460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79745548..79842753hg38UCSC Ensembl
chr10:81505304..81602509hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3897206
hg1997206
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623925
Supporting Variants
SamplesNA18631
Known GenesLOC642361
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13870187
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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