A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602559



Internal ID6989592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145353203..145368955hg38UCSC Ensembl
Innerchr4:145353353..145368805hg38UCSC Ensembl
Outerchr4:145353053..145369105hg38UCSC Ensembl
chr4:146274355..146290107hg19UCSC Ensembl
Innerchr4:146274505..146289957hg19UCSC Ensembl
Outerchr4:146274205..146290257hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3815753
hg1915753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11641087, essv11641085, essv11641083, essv11641084, essv11641088, essv11641089, essv11641086
SamplesHG01624, HG01531, HG01522, NA19725, HG01345, HG01675, NA07056
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602559
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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