A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13733599



Internal ID3735416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27569543..27704372hg38UCSC Ensembl
chr10:27858472..27993301hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38134830
hg19134830
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622728
Supporting Variants
SamplesHG00631
Known GenesMKX
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13733599
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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