A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13979665



Internal ID6011022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131608130..131730858hg38UCSC Ensembl
chr10:133440466..133563194hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38122729
hg19122729
Variant TypeCNV gain
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624963
Supporting Variants
SamplesNA19428
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13979665
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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