A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11765177



Internal ID1766993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:74460..122563hg38UCSC Ensembl
chr5:74575..122678hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3848104
hg1948104
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3603727
Supporting Variants
SamplesHG04033
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11765177
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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