A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13697859



Internal ID3699675
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622393
Supporting Variants
SamplesHG02679
Known GenesCCDC3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13697859
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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