A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13882182



Internal ID1716914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:85034780..85263183hg38UCSC Ensembl
chr10:86794536..87022939hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38228404
hg19228404
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624058
Supporting Variants
SamplesHG01597
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13882182
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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