A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11871385



Internal ID4905217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:38165602..38201570hg38UCSC Ensembl
chr5:38165704..38201672hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3835969
hg1935969
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3604763
Supporting Variants
SamplesNA12717
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11871385
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