A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13941206



Internal ID6025785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113520488..113541946hg38UCSC Ensembl
chr10:115280247..115301705hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3821459
hg1921459
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624602
Supporting Variants
SamplesNA19435
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13941206
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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