A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13913276



Internal ID6189114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101510860..101643510hg38UCSC Ensembl
chr10:103270617..103403267hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38132651
hg19132651
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624382
Supporting Variants
SamplesNA19722
Known GenesBTRC, DPCD, FBXW4, MIR3158-1, MIR3158-2, POLL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13913276
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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