A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8922232



Internal ID14865769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174015173..174015207hg38UCSC Ensembl
Innerchr4:174015186..174015191hg38UCSC Ensembl
Outerchr4:174015155..174015225hg38UCSC Ensembl
chr4:174936324..174936358hg19UCSC Ensembl
Innerchr4:174936337..174936342hg19UCSC Ensembl
Outerchr4:174936306..174936376hg19UCSC Ensembl
chr4:175172899..175172933hg18UCSC Ensembl
Innerchr4:175172917..175172912hg18UCSC Ensembl
Outerchr4:175172881..175172951hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38272
hg19272
hg18272
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3397819
Supporting Variants
SamplesNA19114
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8922232
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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