A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602759



Internal ID6989792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155451344..155452893hg38UCSC Ensembl
Innerchr4:155451384..155452854hg38UCSC Ensembl
Outerchr4:155451305..155452933hg38UCSC Ensembl
chr4:156372496..156374045hg19UCSC Ensembl
Innerchr4:156372536..156374006hg19UCSC Ensembl
Outerchr4:156372457..156374085hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg381550
hg191550
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11659243, essv11659241, essv11659245, essv11659246, essv11659244, essv11659242
SamplesNA18999, NA19086, NA18948, NA19084, NA18945, NA18972
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602759
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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