A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13468696



Internal ID3470512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:39140769..39206562hg38UCSC Ensembl
chr9:39140766..39206559hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3865794
hg1965794
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620452
Supporting Variants
SamplesHG00404
Known GenesCNTNAP3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13468696
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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