A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622754



Internal ID7009612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28700413..28740756hg38UCSC Ensembl
chr10:28989342..29029685hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3840344
hg1940344
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13738677
SamplesHG03736
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622754
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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