A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13664669



Internal ID3833809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:953857..983237hg38UCSC Ensembl
chr10:999797..1029177hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3829381
hg1929381
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622094
Supporting Variants
SamplesHG03470
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13664669
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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