A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622393



Internal ID6662563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12992991..13015357hg38UCSC Ensembl
chr10:13034991..13057357hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3822367
hg1922367
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13697859, essv13697858
SamplesHG01464, HG02679
Known GenesCCDC3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622393
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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