A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13732569



Internal ID3734385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27206246..27213897hg38UCSC Ensembl
chr10:27495175..27502826hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg387652
hg197652
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622710
Supporting Variants
SamplesHG04164
Known GenesACBD5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13732569
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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