A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14909850



Internal ID4911667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113971705..114135826hg38UCSC Ensembl
chr13:114741116..114901301hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38164122
hg19160186
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633629
Supporting Variants
SamplesHG00739
Known GenesRASA3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14909850
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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