A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631834



Internal ID7018643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39484395..39496505hg38UCSC Ensembl
chr13:40058532..40070642hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3812111
hg1912111
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv327e214
Supporting Variantsessv14702945
SamplesNA18965
Known GenesLHFP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631834
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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