A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602584



Internal ID6642840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:146683951..146768781hg38UCSC Ensembl
Innerchr4:146683991..146768741hg38UCSC Ensembl
Outerchr4:146683911..146768821hg38UCSC Ensembl
chr4:147605103..147689933hg19UCSC Ensembl
Innerchr4:147605143..147689893hg19UCSC Ensembl
Outerchr4:147605063..147689973hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg3884831
hg1984831
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11645842
SamplesHG03439
Known GenesTTC29
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602584
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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