A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13749840



Internal ID6066495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31965722..31981938hg38UCSC Ensembl
chr10:32254650..32270866hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3816217
hg1916217
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622820
Supporting Variants
SamplesNA19456
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13749840
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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