A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14820065



Internal ID4193162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:81952185..82016541hg38UCSC Ensembl
chr13:82526320..82590676hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3864357
hg1964357
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3632878
Supporting Variants
SamplesHG03781
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14820065
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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