A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15826011



Internal ID4862950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:27065058..27088810hg38UCSC Ensembl
chr18:24645022..24668774hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3823753
hg1923753
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3642035
Supporting Variants
SamplesNA12286
Known GenesCHST9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15826011
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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