A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633629



Internal ID6673750
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14909850
SamplesHG00739
Known GenesRASA3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633629
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer