A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633239



Internal ID6673361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95128901..95130790hg38UCSC Ensembl
Innerchr13:95128901..95130790hg38UCSC Ensembl
Outerchr13:95128718..95131024hg38UCSC Ensembl
chr13:95781155..95783044hg19UCSC Ensembl
Innerchr13:95781155..95783044hg19UCSC Ensembl
Outerchr13:95780972..95783278hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg381890
hg191890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14868829, essv14868832, essv14868830, essv14868831
SamplesHG02808, NA18511, NA20298, NA19350
Known GenesABCC4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633239
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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