A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622094



Internal ID7008953
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv89e214
Supporting Variantsessv13664668, essv13664669
SamplesHG02568, HG03470
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622094
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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