A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601620



Internal ID6988656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102662459..102663093hg38UCSC Ensembl
Innerchr4:102662502..102663050hg38UCSC Ensembl
Outerchr4:102662416..102663136hg38UCSC Ensembl
chr4:103583616..103584250hg19UCSC Ensembl
Innerchr4:103583659..103584207hg19UCSC Ensembl
Outerchr4:103583573..103584293hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38635
hg19635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11547852
SamplesHG04222
Known GenesMANBA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601620
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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