A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603817



Internal ID6644071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1638442..1833414hg38UCSC Ensembl
chr5:1638557..1833528hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38194973
hg19194972
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11784540, essv11784539, essv11784541
SamplesNA18977, HG03166, HG00581
Known GenesMIR4277, MRPL36, NDUFS6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603817
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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