A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12102835



Internal ID4410521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152941676..153029735hg38UCSC Ensembl
chr5:152321236..152409295hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3888060
hg1988060
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3607213
Supporting Variants
SamplesHG03926
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12102835
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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