A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611123



Internal ID6998034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144866601..144954099hg38UCSC Ensembl
chr6:145187737..145275235hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3887499
hg1987499
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12576252
SamplesHG00631
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611123
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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