A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603213



Internal ID6643469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173545438..173555636hg38UCSC Ensembl
Innerchr4:173545452..173555622hg38UCSC Ensembl
Outerchr4:173545424..173555650hg38UCSC Ensembl
chr4:174466589..174476787hg19UCSC Ensembl
Innerchr4:174466603..174476773hg19UCSC Ensembl
Outerchr4:174466575..174476801hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3810199
hg1910199
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11707438, essv11707439
SamplesNA19027, NA19395
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603213
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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