A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14888832



Internal ID6571715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:105301098..105304219hg38UCSC Ensembl
chr13:105953449..105956570hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg383122
hg193122
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633442
Supporting Variants
SamplesNA20760
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14888832
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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