A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602723



Internal ID6989756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153369645..153372444hg38UCSC Ensembl
Innerchr4:153369646..153372444hg38UCSC Ensembl
Outerchr4:153369645..153372445hg38UCSC Ensembl
chr4:154290797..154293596hg19UCSC Ensembl
Innerchr4:154290798..154293596hg19UCSC Ensembl
Outerchr4:154290797..154293597hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11655748, essv11655749, essv11655747, essv11655746, essv11655745, essv11655744
SamplesHG03897, HG00365, HG03780, HG00320, HG00378, HG00329
Known GenesMND1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602723
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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