A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603109



Internal ID6643365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168797160..168797972hg38UCSC Ensembl
Innerchr4:168797164..168797969hg38UCSC Ensembl
Outerchr4:168797157..168797976hg38UCSC Ensembl
chr4:169718311..169719123hg19UCSC Ensembl
Innerchr4:169718315..169719120hg19UCSC Ensembl
Outerchr4:169718308..169719127hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38813
hg19813
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11687757, essv11687754, essv11687755, essv11687761, essv11687758, essv11687760, essv11687756, essv11687759, essv11687763, essv11687762, essv11687753, essv11687764
SamplesNA19209, HG01915, NA19474, HG02583, HG02703, HG03391, NA19704, HG02624, HG02484, HG02589, HG02855, HG03460
Known GenesPALLD
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603109
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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