A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601657



Internal ID6988693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:105012463..105162253hg38UCSC Ensembl
Innerchr4:105012463..105162253hg38UCSC Ensembl
Outerchr4:105011963..105162753hg38UCSC Ensembl
chr4:105933620..106083410hg19UCSC Ensembl
Innerchr4:105933620..106083410hg19UCSC Ensembl
Outerchr4:105933120..106083910hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38149791
hg19149791
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11552893
SamplesHG03366
Known GenesTET2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601657
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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