A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13695229



Internal ID664172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:10088921..10130504hg38UCSC Ensembl
chr10:10130884..10172467hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3841584
hg1941584
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622320
Supporting Variants
SamplesHG00309
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13695229
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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